Peptide-mimetic hydrogels as a long-acting multipurpose drug delivery platform for combined contraception and HIV prevention
Lead Research Organisation:
Queen's University Belfast
Department Name: Sch of Pharmacy
Abstract
HIV/AIDS is the leading cause of death in women of reproductive age worldwide. HIV and unintended pregnancies are prevalent in developing nations due to the lack of effective female contraceptive choice. HIV/AIDs remains one of the key challenges facing the UK (428 deaths from AIDS-related illnesses in 2017) and our rate of unintended pregnancies are the highest in Western Europe (one in six pregnancies). One of the key issues is that patients struggle to adhere to the complex regimens of HIV and contraceptive therapies, which often require multiple dosing at very specific times each day. Recent strategies have focused on solving patient adherence issues by using long-acting injectable technologies. However, such products have several significant issues that limit their wider use as combined HIV and contraceptive therapies, such as:
-the use of water-insoluble drugs that limit the type of drugs that can be incorporated into the product meaning a dual HIV-contraceptive technology is difficult to achieve
-fast drug release after insertion leading to potential toxicity issues/concerns over dose received
-a need for surgery for implant insertion and removal
-a requirement for large needles
-stability issues upon storage/transport to the developing world which can result in clogging of syringes and incomplete dosing of drugs.
Our project aims to overcome these issues by creating a soluble injection of enhanced stability, for improved ease of administration under the skin. This will form a hydrogel implant in response to enzymes present within the skin to release drugs long-term, removing the need for daily dosing. Our injectable implant is composed of peptide-like molecules which are capable of forming tissue-like hydrogels that can be tailored to gradually release drugs for at least 28 days. This will remove the need for patients to comply with complex drug dosing regimens on a daily basis and improve their adherence to medication. Natural peptides form the building blocks of proteins and tissues. Their use as a drug releasing hydrogel implant for administration under the skin is promising due to their high biocompatibility, but limited by their rapid degradation within hours by enzymes present in the human body. This project overcomes stability issues by studying peptide-mimetics, which retain the positive properties of peptides (e.g. biocompatibility, easy drug attachment) with the ability to form hydrogels that will be stable for the duration of therapy. Peptide-mimetics can be tailored to degrade within the body over months into non-toxic components that are eliminated from the patient, meaning surgical removal is not necessary.
Our peptide-mimetics possess high chemical versatility (i.e. wide choice of chemical functional groups). Therefore multiple drugs can be attached directly to the peptide-mimetic hydrogel enabling large quantities of drug to be incorporated to meet in vivo therapeutic need for at least 28 days. Drug detachment proceeds in physiological conditions after the hydrogel forms reducing potential for rapid burst release of drug upon injection. Drug release studies will assess the potential for sustained drug administration in a bid to minimise pharmacokinetic peaks and troughs in drug concentrations. The peptide-mimetics studied in this project are purposefully small molecules that are cheap to manufacture, improving their potential to be clinically translated as a pharmaceutical product and effectively utilised within healthcare budgets for patient and societal benefit.
The data obtained will allow the practical utility of this peptide-mimetic hydrogel approach to long-acting injectable administration of drugs to be assessed. This platform has high potential to be adopted as a novel implant for the sustained delivery of drugs for conditions where patients have difficulty adhering to their medicines (e.g. Alzheimer's, tuberculosis, depression, schizophrenia, malaria).
-the use of water-insoluble drugs that limit the type of drugs that can be incorporated into the product meaning a dual HIV-contraceptive technology is difficult to achieve
-fast drug release after insertion leading to potential toxicity issues/concerns over dose received
-a need for surgery for implant insertion and removal
-a requirement for large needles
-stability issues upon storage/transport to the developing world which can result in clogging of syringes and incomplete dosing of drugs.
Our project aims to overcome these issues by creating a soluble injection of enhanced stability, for improved ease of administration under the skin. This will form a hydrogel implant in response to enzymes present within the skin to release drugs long-term, removing the need for daily dosing. Our injectable implant is composed of peptide-like molecules which are capable of forming tissue-like hydrogels that can be tailored to gradually release drugs for at least 28 days. This will remove the need for patients to comply with complex drug dosing regimens on a daily basis and improve their adherence to medication. Natural peptides form the building blocks of proteins and tissues. Their use as a drug releasing hydrogel implant for administration under the skin is promising due to their high biocompatibility, but limited by their rapid degradation within hours by enzymes present in the human body. This project overcomes stability issues by studying peptide-mimetics, which retain the positive properties of peptides (e.g. biocompatibility, easy drug attachment) with the ability to form hydrogels that will be stable for the duration of therapy. Peptide-mimetics can be tailored to degrade within the body over months into non-toxic components that are eliminated from the patient, meaning surgical removal is not necessary.
Our peptide-mimetics possess high chemical versatility (i.e. wide choice of chemical functional groups). Therefore multiple drugs can be attached directly to the peptide-mimetic hydrogel enabling large quantities of drug to be incorporated to meet in vivo therapeutic need for at least 28 days. Drug detachment proceeds in physiological conditions after the hydrogel forms reducing potential for rapid burst release of drug upon injection. Drug release studies will assess the potential for sustained drug administration in a bid to minimise pharmacokinetic peaks and troughs in drug concentrations. The peptide-mimetics studied in this project are purposefully small molecules that are cheap to manufacture, improving their potential to be clinically translated as a pharmaceutical product and effectively utilised within healthcare budgets for patient and societal benefit.
The data obtained will allow the practical utility of this peptide-mimetic hydrogel approach to long-acting injectable administration of drugs to be assessed. This platform has high potential to be adopted as a novel implant for the sustained delivery of drugs for conditions where patients have difficulty adhering to their medicines (e.g. Alzheimer's, tuberculosis, depression, schizophrenia, malaria).
Planned Impact
The beneficiaries from this project are the following:
Academia and Business/Industry: Our platform has high potential to be scalable by the pharmaceutical industry and distributed worldwide. Our project will bring international investment, commercialisation and knowledge exploitation to the UK in a key area, i.e. healthcare (see letter of support Merck). It will advance the EPSRC's goals aligning with the aims of their Future Manufacturing Hub in Targeted Healthcare and their current portfolios (see Case for Support: National Importance). Benefits to QUB are increased recognition as a leading university for knowledge exchange and commercialisation of our platform via patents and industrial investment. Our project will generate data key to product development, important for clinical trials and commercialisation via the pharmaceutical industry.
Impact on society: Our project will test the feasibility of a single long-acting product that simultaneously targets contraception and HIV. It will have lasting impact, addressing family planning and HIV prevention and empowering women to take control of their sexual health worldwide. Current therapies fail to address the global burden of HIV transmission and provision of contraception due to poor patient compliance with complicated treatment regimens and the limitations of existing formulations. Our technology will overcome such barriers by providing therapeutic coverage for greater than 28 days within a single injection. Our research will inform national (MHRA) and international (FDA) policy makers with regard to regulation of peptide-mimetics. It will provide a valuable alternative to healthcare professionals involved in HIV and contraceptive provision. It will aid in preventing HIV development and improve compliance with therapy, thereby limiting HIV antimicrobial resistance. Our research will increase political interest in developing new medical therapies, especially within the theme of drug delivery. It will provide evidence that effective legislation is addressing both the HIV crisis and improved contraceptive choice worldwide, positively influencing policies towards funding of health services, medical research and education.
Impact on people: The Research Fellows and the research team will enhance their skills in multiple disciplines (chemistry, biology, physics, pharmaceutics, project management) by being involved within project meetings and all stages of product development. The Research Fellows will increase their employability (e.g. papers, conferences) for a future role within academia or industry.
Impact on economy: This project will significantly contribute to the prevention of HIV and unwanted pregnancies, a large burden on economies worldwide. This technology will contribute substantially to the UN's Goals of: improving maternal reproductive health; combating HIV and preventing sexually transmitted infections; good health and gender equality. It will increase the UK's reputation in research, resulting in economic prosperity and increased employment within healthcare.
Dissemination and communication: Other beneficiaries include the general public, charities (e.g. Positive Life NI), students and those involved in STEM education. Our project will improve teaching within UK higher and secondary education, serving as a case study for materials research, leading to improvement in research skills within the population and increased public engagement in research and education. The W5 Science museum Belfast will benefit from annual talks and we will aim to develop a permanent case study. Students (PhD, MSc, BSc) at QUB will benefit from sharing of knowledge from the research team through e.g. lectures. Undergraduates will benefit from engaging in lab projects and summer studentships (e.g. paper authorship). This will increase their employability via direct experience of a multi-disciplinary project, increasing their enthusiasm for a career in the STEM sector.
Academia and Business/Industry: Our platform has high potential to be scalable by the pharmaceutical industry and distributed worldwide. Our project will bring international investment, commercialisation and knowledge exploitation to the UK in a key area, i.e. healthcare (see letter of support Merck). It will advance the EPSRC's goals aligning with the aims of their Future Manufacturing Hub in Targeted Healthcare and their current portfolios (see Case for Support: National Importance). Benefits to QUB are increased recognition as a leading university for knowledge exchange and commercialisation of our platform via patents and industrial investment. Our project will generate data key to product development, important for clinical trials and commercialisation via the pharmaceutical industry.
Impact on society: Our project will test the feasibility of a single long-acting product that simultaneously targets contraception and HIV. It will have lasting impact, addressing family planning and HIV prevention and empowering women to take control of their sexual health worldwide. Current therapies fail to address the global burden of HIV transmission and provision of contraception due to poor patient compliance with complicated treatment regimens and the limitations of existing formulations. Our technology will overcome such barriers by providing therapeutic coverage for greater than 28 days within a single injection. Our research will inform national (MHRA) and international (FDA) policy makers with regard to regulation of peptide-mimetics. It will provide a valuable alternative to healthcare professionals involved in HIV and contraceptive provision. It will aid in preventing HIV development and improve compliance with therapy, thereby limiting HIV antimicrobial resistance. Our research will increase political interest in developing new medical therapies, especially within the theme of drug delivery. It will provide evidence that effective legislation is addressing both the HIV crisis and improved contraceptive choice worldwide, positively influencing policies towards funding of health services, medical research and education.
Impact on people: The Research Fellows and the research team will enhance their skills in multiple disciplines (chemistry, biology, physics, pharmaceutics, project management) by being involved within project meetings and all stages of product development. The Research Fellows will increase their employability (e.g. papers, conferences) for a future role within academia or industry.
Impact on economy: This project will significantly contribute to the prevention of HIV and unwanted pregnancies, a large burden on economies worldwide. This technology will contribute substantially to the UN's Goals of: improving maternal reproductive health; combating HIV and preventing sexually transmitted infections; good health and gender equality. It will increase the UK's reputation in research, resulting in economic prosperity and increased employment within healthcare.
Dissemination and communication: Other beneficiaries include the general public, charities (e.g. Positive Life NI), students and those involved in STEM education. Our project will improve teaching within UK higher and secondary education, serving as a case study for materials research, leading to improvement in research skills within the population and increased public engagement in research and education. The W5 Science museum Belfast will benefit from annual talks and we will aim to develop a permanent case study. Students (PhD, MSc, BSc) at QUB will benefit from sharing of knowledge from the research team through e.g. lectures. Undergraduates will benefit from engaging in lab projects and summer studentships (e.g. paper authorship). This will increase their employability via direct experience of a multi-disciplinary project, increasing their enthusiasm for a career in the STEM sector.
Publications
Huwaitat R
(2020)
Antibacterial and antibiofilm efficacy of synthetic polymyxin-mimetic lipopeptides
in Peptide Science
Pentlavalli S
(2024)
D-peptide hydrogels as a long-acting multipurpose drug delivery platform for combined contraception and HIV prevention.
in Journal of controlled release : official journal of the Controlled Release Society
Coulter SM
(2023)
Enzyme-Triggered l-a/d-Peptide Hydrogels as a Long-Acting Injectable Platform for Systemic Delivery of HIV/AIDS Drugs.
in Advanced healthcare materials
Laverty G
(2025)
Hydrogels in Drug Delivery
Moore J
(2024)
Impact of counterion and salt form on the properties of long-acting injectable peptide hydrogels for drug delivery
in Faraday Discussions
Coulter SM
(2024)
In Situ Forming, Enzyme-Responsive Peptoid-Peptide Hydrogels: An Advanced Long-Acting Injectable Drug Delivery System.
in Journal of the American Chemical Society
| Description | This work has led to the development of a new advanced drug delivery system that is composed of peptide-like molecules (peptoid-peptides) that mimic the structure and properties of human tissues, forming hydrogels. The structure elucidated is novel and was selected by screening several different peptide-like compounds for their ability to form hydrogels in response to specific enzymes (phosphatases) that exist within the human body. This project has focused on using this technology to deliver multiple drugs within one injectable platform, in order to provide discreet HIV prevention and contraceptive protection to women. New multipurpose technologies controlled by women, focused on reducing HIV infections and preventing unwanted pregnancies are a global health priority according to the World Health Organization and the UN Millennium/Sustainable Development Goals. This system holds promise in other areas were sustained drug release may be beneficial e.g., cancer, tuberculosis, malaria, infectious disease, medical device infections, ocular and central nervous system delivery, substance abuse and mental health disorders. We envisage clinical peptoid-peptide products to be formulated as powders for injection to provide sufficient pharmaceutical stability and shelf-life. Therefore, optimizing the freeze-dried preparation and sterilisation of this powder formulation , establishing long-term stability, and ensuring that it is readily reconstituted in buffer/water prior to administration as a sterile product will be important. We have demonstrated peptoid-peptide can deliver drugs systemically (to blood) after injection under the skin (subcutaneous) to clinically relevant concentrations for at least 50 days. We have generated a significant proof-of-concept data package comprising chemical synthesis (to lower gram scale), mechanical properties (oscillatory rheology), structure (microscopy, circular dichroism, neutron scattering), biostability, cell toxicity and drug release. We have also gathered preliminary patient feedback on our approach in collaboration with local HIV charity Positive Life NI. A patent application has been submitted to the UK Patent Office (2304871.3) with a PCT application currently being developed. Commercial exploitation of our technology is therefore a real possibility. This project has also enabled new collaborations to be established with important external partners including the use of neutron scattering facilities at ISIS UK Neutron and Muon Source and Institut Laue-Langevin (ILL) Grenoble France. |
| Exploitation Route | Peptoid-peptides also hold significant promise as new materials for wider use in areas where synthetic and peptide hydrogels are being applied e.g., 3D cell culture, biosensors, wound healing, 3D printing, and stem cell and gene cell delivery. |
| Sectors | Chemicals Healthcare Manufacturing including Industrial Biotechology Pharmaceuticals and Medical Biotechnology |
| URL | https://webarchive.nationalarchives.gov.uk/ukgwa/20210701095331/http://epsrc.ukri.org/files/research/gel-injections |
| Description | Expert Member on the British Pharmacopoeia Commission's Biological and Biotechnological Products Expert Advisory Group |
| Geographic Reach | National |
| Policy Influence Type | Participation in a guidance/advisory committee |
| Impact | This work involves setting Pharmacopoeial Monographs which directly impact safety, quality and efficacy of medicines, particularly biologics in humans and animals. |
| URL | https://www.pharmacopoeia.com/about-us/the-bp/meet-the-team |
| Description | Invited Discussion Leader. Gordon Research Conference: Peptide Materials: Molecule Design, Self-Assembly, Material Structure, Biomaterials, Biomimicry, and Other Advances, Pomona, California, USA, 19th - 24th January 2025. |
| Geographic Reach | Multiple continents/international |
| Policy Influence Type | Influenced training of practitioners or researchers |
| URL | https://www.grc.org/peptide-materials-conference/2025/ |
| Description | Universidade do Porto: External teaching on Advanced Training Course in Molecular Bioengineering: Supramolecular Peptide Hydrogels |
| Geographic Reach | Europe |
| Policy Influence Type | Contribution to new or improved professional practice |
| Impact | These students will go on to perform PhDs and work in industry. The teaching I have provided should therefore inform their practice e.g. in the design and development of advanced drug delivery systems. |
| URL | https://www.i3s.up.pt/training-detail.php?v=283#:~:text=The%20course%20is%20designed%20for,doctoral%... |
| Description | Drug release kinetics & water diffusion in a long-acting peptide hydrogel drug delivery implant for combined contraception & HIV prevention |
| Amount | £75,000 (GBP) |
| Funding ID | No 8-04-935 |
| Organisation | Institut Laue–Langevin |
| Sector | Academic/University |
| Country | France |
| Start | 12/2022 |
| End | 05/2023 |
| Description | ISIS beamtime application standard mode |
| Amount | £30,000 (GBP) |
| Funding ID | RB2310068 |
| Organisation | Science and Technologies Facilities Council (STFC) |
| Sector | Public |
| Country | United Kingdom |
| Start | 01/2023 |
| End | 07/2023 |
| Description | ISIS beamtime application standard mode. Understanding water diffusion and release kinetics in long-acting peptide hydrogel drug delivery implants. |
| Amount | £90,000 (GBP) |
| Funding ID | RB2220032 |
| Organisation | Science and Technologies Facilities Council (STFC) |
| Sector | Public |
| Country | United Kingdom |
| Start | 06/2022 |
| End | 04/2023 |
| Description | Innovation-to-Commercialisation of University Research (ICURe) SETsquared Award Cohort 32 License & Collaboration Follow-on Programme. Innovative hydrogels for agriculture |
| Amount | £15,420 (GBP) |
| Funding ID | 32-08/520268133 |
| Organisation | Innovate UK |
| Sector | Public |
| Country | United Kingdom |
| Start | 03/2021 |
| End | 06/2021 |
| Description | Invest NI Proof of Concept: A peptide hydrogel implant technology to improve patient adherence to HIV/AIDs drugs. |
| Amount | £125,827 (GBP) |
| Funding ID | 2111/130282815 |
| Organisation | Invest Northern Ireland |
| Sector | Public |
| Country | United Kingdom |
| Start | 11/2021 |
| End | 05/2023 |
| Description | Neutron beam time allocation standard mode: Using rheo-SANS to monitor the structure of in situ forming peptide-like hydrogel drug delivery implants |
| Amount | £30,000 (GBP) |
| Funding ID | No 9-13-1100 |
| Organisation | Institut Laue–Langevin |
| Sector | Academic/University |
| Country | France |
| Start | 07/2023 |
| End | 08/2023 |
| Description | PATH, MATRIX Technology Accelerator Domain 1 RFA2024-003. SLIPI - Silicone personal lubricants for HIV prevention. |
| Amount | $149,018 (USD) |
| Organisation | United States Agency for International Development |
| Sector | Public |
| Country | United States |
| Start | 11/2024 |
| End | 07/2026 |
| Description | The Institut Laue-Langevin (ILL) neutron beam time allocation standard mode. Understanding the microscopic properties and drug diffusion kinetics of long-acting peptoid-peptide drug delivery implants for HIV/AIDs. Garry Laverty (PI), Emily Cross (CI) |
| Amount | £30,000 (GBP) |
| Funding ID | No 9-13-972 |
| Organisation | Institut Laue–Langevin |
| Sector | Academic/University |
| Country | France |
| Start | 05/2021 |
| End | 06/2021 |
| Description | The Queen's University of Belfast Confidence in Concept programme 2018/19 |
| Amount | £67,867 (GBP) |
| Funding ID | MC_PC_18060 |
| Organisation | Medical Research Council (MRC) |
| Sector | Public |
| Country | United Kingdom |
| Start | 06/2019 |
| End | 06/2022 |
| Description | UKRI Innovate UK ICURe SETsquared Award Cohort 32 |
| Amount | £30,000 (GBP) |
| Funding ID | 32-08 / 520268133 |
| Organisation | Queen's University Belfast |
| Sector | Academic/University |
| Country | United Kingdom |
| Start | 01/2021 |
| End | 03/2021 |
| Title | Dataset for "Enzyme triggered L-a/D-peptide hydrogels as a long-acting injectable delivery platform for HIV/AIDS" |
| Description | Data relates to a formulation composed of a self-assembling ultrashort D or L peptide hydrogelator, namely phosphorylated (naphthalene-2-ly)-acetyl-diphenylalanine-lysine-tyrosine-OH (NapFFKY[p]-OH), to which zidovudine is conjugated covalently . Data includes rheological analysis, small angle neutron scattering, resistance to protease degradation (biostability), cell toxicity and drug release (both in vitro and in vivo). Paper abstract: Eradicating HIV/AIDS by 2030 is a central goal of the World Health Organization. Key to addressing this challenge is overcoming issues patients have with adhering to their medicines. This includes a commitment to complicated drug dosage regimens, for example a daily intake of tablets at very specific times. There is a clear need for a convenient and effective long-acting formulation to deliver drugs to patients over a sustained period. This paper aims to develop an injectable in situ forming hydrogel implant for the delivery of a model HIV/AIDS antiretroviral drug (zidovudine) over 28 days. The formulation is composed of a self-assembling ultrashort D or L-? peptide hydrogelator, namely phosphorylated (naphthalene-2-ly)-acetyl-diphenylalanine-lysine-tyrosine-OH (NapFFKY[p]-OH), to which zidovudine is conjugated covalently via an ester linkage. This platform is formulated as a powder that can be readily dissolved in aqueous buffer to form an injectable antiretroviral-peptide solution. Using rheological analysis, peptides demonstrated enzyme instructed self-assembly, forming hydrogels within minutes in the presence of phosphatase enzyme. Small angle neutron scattering suggest peptide gels form fibres of narrow radius (~2 nm) and large length, closely fitting the flexible cylinder elliptical model. D-peptides were particularly promising as a long-acting drug delivery platform, displaying resistance to protease degradation for 28 days. Drug release, via hydrolysis of the drug-peptide ester linkage, was shown to progress under physiological conditions (37 ?C, pH 7.4, H2O). In vivo studies in Sprague Dawley rats demonstrated zidovudine blood plasma concentrations to be within IC50 range (30 - 130 ng/mL) for 35 days after subcutaneous administration of Napffk(AZT)Y[p]G-OH. This work is a proof-of-concept for the development of a long-acting combined injectable in situ forming implant using a peptide hydrogel formulation strategy. A successful single, long-acting, highly user-adherent product that targets HIV/AIDS is a high priority due to the positive societal, health and economic impact this technology would provide. |
| Type Of Material | Database/Collection of data |
| Year Produced | 2022 |
| Provided To Others? | Yes |
| Impact | Research manuscript submitted, currently under review |
| URL | https://pure.qub.ac.uk/en/datasets/dataset-for-enzyme-triggered-l-%CE%B1d-peptide-hydrogels-as-a-lon... |
| Title | Dataset for "Impact of counterion and salt form on the properties of long-acting injectable peptide hydrogels for drug delivery" |
| Description | Dataset for paper entitled "Impact of counterion and salt form on the properties of long-acting injectable peptide hydrogels for drug delivery". Abstract for paper: Modifying the salt form of active pharmaceutical ingredients is a common method to enhance their physicochemical and biological properties, whilst improving their abiliy to be formulated into medicines that can be effectively delivered to patients. Salts and counterions are especially relevant to peptide therapies given that the majority of low molecular weight peptides synthesised by solid-phase protocols form a trifluoroacetate (TFA) salt due to the use of trifluoroacetic acid in resin cleaving and follow-on purification methods. TFA salts are not viewed as favourably by medicine regulators and can be defined as a new chemical entity entirely due to their different biological and physicochemical properties. Despite some exceptions, the vast majority of therapeutic peptides are marketed as hydrochloride (HCl) or acetate salts, even though most early research and development is centred on TFA salts. The aim of study was to compare the impact of salt form (TFA vs. HCl) on the biostability, cell cytotoxicity, drug release and rheological properties of a Napffky(p)G-OH peptide hydrogel platform that demonstrates promise as a long-acting drug delivery system. This study demonstrated no significant difference between the salt forms for properties important to its intended use. This paper also raises important points for discussion relating to the environmental and regulatory status of peptide salts and their use as pharmaceuticals. Dataset information: There is an urgent need for new long-acting formulations to improve patient access and adherence to medicines. Several marketed long-acting injectable nanosuspensions comprising water-insoluble drugs are utilised for treatment of schizophrenia and for pre-exposure prophylaxis (PrEP) against HIV infection. In situ forming peptide and peptide-like hydrogels hold significant promise to overcome some of the disadvantages associated with existing nanosuspension injections including: the need for water-insoluble drugs; challenges encountered incorporating multiple drugs within one injectable product; the formation of amorphous drug during milling; and difficulties relating to large-scale manufacture. The majority of peptides synthesised by solid-phase protocols result in a trifluoroacetate salt due to the use of trifluoroacetic acid in resin cleaving and purification steps. Trifluoroacetate salts are not viewed favourably by Medicine regulators e.g. MHRA, FDA, EMA, and are commonly defined as a new chemical entity entirely due to their impact on the biological and physicochemical properties of peptides. Therefore the vast majority of therapeutic peptides are marketed as hydrochloride (HCl) or acetate salts. Despite this, the vast majority of early research and development is centred on TFA salts. The aim of study was to compare the impact of HCl salt conversion on the biostability, cell cytotoxicity, drug release and rheological properties of our Napffky(p)G-OH peptide hydrogel platform. All files provide a comparison of data for (naphthalene-2-ly)-acetyl-D-phenylalanine-D-phenylalanine-D-lysine-phosphorylated D-tyrosine-glycine-OH (Napffky(p)G-OH) in both HCl and TFA salt forms. Studies were conducted and data generated using the equipment and methods outlined within the readme file (Combined Institutional readme file for Impact of counterion and salt form on the properties dataset in Pure) at the School of Pharmacy, Queen's University Belfast between 20/07/20 and 30/09/24. This data is likely to be of relevance to researchers working within the pharmaceutical and drug delivery field. Especially those with an interest in the impact of different salt forms of drugs on their properties and those involved in the development of peptide medicines and peptide-based materials. More specific details in relation to the source and definition of data is outlined within the readme file entitled "Combined Institutional readme file for Impact of counterion and salt form on the properties dataset in Pure." Only one readme file is used to define this dataset. This dataset contains: Biostability.csv This file relates to the biostability of (naphthalene-2-ly)-acetyl-D-phenylalanine-D-phenylalanine-D-lysine-phosphorylated D-tyrosine-glycine-OH (Napffky(p)G-OH) in both HCl and TFA salt forms against the protease enzyme proteinase K for 28 day time period. Frequency sweeps rheology.csv Strain sweeps rheology.csv Time sweeps rheology.csv These files relates to the oscillatory rheological properties of (naphthalene-2-ly)-acetyl-D-phenylalanine-D-phenylalanine-D-lysine-phosphorylated D-tyrosine-glycine-OH (Napffky(p)G-OH) in both HCl and TFA salt forms. Frequency sweeps provide an indication of gel formation via storage modulus G' and loss modulus G'' measurements. Strain sweeps provide an indication of gel strength and time sweeps demonstrate time for gelation in response to phosphatase enzyme. MTS 6 hours.csv MTS 24 hours.csv MTS 48 hours.csv MTS 72 hours.csv MTS files relate to cell metabolic activity of NCTC 929 cells after stated exposure time (6, 24, 48 and 72 hours) to (naphthalene-2-ly)-acetyl-D-phenylalanine-D-phenylalanine-D-lysine-phosphorylated D-tyrosine-glycine-OH (Napffky(p)G-OH) in both HCl and TFA salt forms. Cabotegravir release.csv This file relates to the drug (cabotegravir) release properties of each peptide gel of (naphthalene-2-ly)-acetyl-D-phenylalanine-D-phenylalanine-D-lysine-phosphorylated D-tyrosine-glycine-OH (Napffky(p)G-OH) in both HCl and TFA salt forms over 28 days. Date made available15 Jan 2025 PublisherQueen's University Belfast Temporal coverage20 Jul 2020 - 30 Sept 2024 Date of data production20 Jul 2020 - 30 Sept 2024 Geographical coverageSchool of Pharmacy, Queen's University Belfast, N. Ireland |
| Type Of Material | Database/Collection of data |
| Year Produced | 2025 |
| Provided To Others? | Yes |
| Impact | Dataset for paper entitled "Impact of counterion and salt form on the properties of long-acting injectable peptide hydrogels for drug delivery." |
| URL | https://pure.qub.ac.uk/en/datasets/dataset-for-impact-of-counterion-and-salt-form-on-the-properties- |
| Title | AN INJECTABLE DELIVERY SYSTEM FOR LONG-ACTING ADMINISTRATION OF DRUGS |
| Description | The invention relates to an injectable delivery system for long-acting administration of drugs. The invention includes a compound formed at least partially from a peptide-mimetic molecule. The compound is configured for the attachment of one or more drug molecules, and is further configured to release the one or more drug molecules under physiological conditions. A solution of the compound forms a hydrogel in response to an enzyme that is endogenous to a human or animal. A solution of the compound can be administered to the skin, wherein upon administration it forms a hydrogel, and any drug attached to the compound is then gradually released. |
| IP Reference | WO2024200593 |
| Protection | Patent / Patent application |
| Year Protection Granted | 2024 |
| Licensed | No |
| Company Name | Resilient Pharma Ltd |
| Description | |
| Year Established | 2023 |
| Impact | N/A awaiting patent approval |
| Description | An article/interview on our research was conducted and published within the leading Irish newspaper: "The Irish Times" |
| Form Of Engagement Activity | A press release, press conference or response to a media enquiry/interview |
| Part Of Official Scheme? | No |
| Geographic Reach | International |
| Primary Audience | Public/other audiences |
| Results and Impact | This was an article as part of Research Insights a series that occurs within the Irish Times enabling scientists to communicate their research activities to a wider audience. |
| Year(s) Of Engagement Activity | 2019 |
| URL | https://www.irishtimes.com/business/innovation/we-can-manipulate-peptides-to-carry-different-medicin... |
| Description | EPSRC Developing Future Therapies Case Study |
| Form Of Engagement Activity | Engagement focused website, blog or social media channel |
| Part Of Official Scheme? | No |
| Geographic Reach | International |
| Primary Audience | Public/other audiences |
| Results and Impact | Our work was highlighted as a case study by the EPSRC on their website for the key EPSRC goal/outcome of "Developing Future Therapies." This enhanced the reputation of researchers involved in the project, our Schools and Institutions. It also lead to contact from interested stakeholders from industry and academic especially. |
| Year(s) Of Engagement Activity | 2021 |
| URL | https://epsrc.ukri.org/files/research/gel-injections/ |
| Description | Featured on Institut Laue-Langevin website, news article: Exciting new material for long-acting drug delivery |
| Form Of Engagement Activity | A magazine, newsletter or online publication |
| Part Of Official Scheme? | No |
| Geographic Reach | International |
| Primary Audience | Public/other audiences |
| Results and Impact | Has resulted in our work being featured in the Institut Laue-Langevin report for 2024 |
| Year(s) Of Engagement Activity | 2024 |
| URL | https://www.ill.eu/infos-presse-evenements/detail-1/exciting-new-material-for-long-acting-drug-deliv... |
| Description | Invited talk Trinity College Dublin Ireland |
| Form Of Engagement Activity | A talk or presentation |
| Part Of Official Scheme? | No |
| Geographic Reach | International |
| Primary Audience | Professional Practitioners |
| Results and Impact | This was an invited talk at the leading University in the Republic of Ireland. The main aim was to disseminate our research to other academics and also postgraduate students as part of a seminar series. There was a series of questions and discussions afterwards. This has lead to increased interest in our research and I am hoping our group will be able to develop further research collaborations from this activity. |
| Year(s) Of Engagement Activity | 2020 |
| Description | Moonshots for the UK: Transforming Tomorrow Together |
| Form Of Engagement Activity | A formal working group, expert panel or dialogue |
| Part Of Official Scheme? | No |
| Geographic Reach | National |
| Primary Audience | Policymakers/politicians |
| Results and Impact | I was invited to pitch a research theme idea to UKRI and DSIT's Moonshots for the UK: Transforming Tomorrow Together event which took place on 1 August 2023 in London. This was chosen from more than 700 ideas from a wide range of people, to support the development of ambitious research and innovation programmes as opportunities arise. |
| Year(s) Of Engagement Activity | 2023 |
| URL | https://www.ukri.org/news/moonshots-for-the-uk-transforming-tomorrow-together/ |
| Description | Northern Ireland Science Festival Talk: Gel Jabs |
| Form Of Engagement Activity | A talk or presentation |
| Part Of Official Scheme? | No |
| Geographic Reach | National |
| Primary Audience | Public/other audiences |
| Results and Impact | Public talk as part of Northern Ireland Science Festival. Details below: How Pioneering Hydrogels Fight Infection and Disease Find out how scientists at Queen's University Belfast are leading the way in the fight against infection and disease with innovative hydrogels which do everything from killing hospital infections to improving how medicine is delivered. Made from peptides - short chains of amino acids known as 'nature's building blocks' - these versatile gels mimic human tissues and are now being used to address the greatest medical challenges. Find out how treatment delivery can be improved by injecting 'peptide-plus-drugs' into the body, forming a drug-releasing gel implant under the skin. This supergel works for several weeks, so patients don't have to take multiple daily pills. Used to deliver antiviral drugs to treat or prevent HIV/AIDS, hydrogels are the next frontier in medicine. |
| Year(s) Of Engagement Activity | 2023 |
| URL | https://nisciencefestival.com/events/gel-jabs |
| Description | Patient and carers talk about our research with Belfast HIV charity Positive Life NI |
| Form Of Engagement Activity | A talk or presentation |
| Part Of Official Scheme? | No |
| Geographic Reach | Regional |
| Primary Audience | Patients, carers and/or patient groups |
| Results and Impact | 20-30 patient, carers and those directly involved in the HIV/AIDS charity Positive LIfe NI joined us for an information session on existing HIV long-acting injectables and our own technology. This took place over zoom due to Covid-19 restrictions. A questions and answers session was provided which stimulated interest in our research and gathered important opinions in our technology which will help guide its future development. |
| Year(s) Of Engagement Activity | 2021 |
| Description | Patient interviews: Positive Life NI Belfast HIV/AIDS charity |
| Form Of Engagement Activity | A talk or presentation |
| Part Of Official Scheme? | No |
| Geographic Reach | Local |
| Primary Audience | Patients, carers and/or patient groups |
| Results and Impact | We conducted interviews with patients with HIV (August-September 2023) to understand their views on our HIV drug delivery technology and how it compares to current treatment approaches. |
| Year(s) Of Engagement Activity | 2023 |
| Description | Podcast: Peptide hydrogel and nanotubes for drug delivery and biomaterial applications |
| Form Of Engagement Activity | A broadcast e.g. TV/radio/film/podcast (other than news/press) |
| Part Of Official Scheme? | No |
| Geographic Reach | International |
| Primary Audience | Media (as a channel to the public) |
| Results and Impact | I presented a live podcast with the science channel ResearcherLive! on our peptide based research and its use in medicine. |
| Year(s) Of Engagement Activity | 2022 |
| URL | https://live.researcher-app.com/peptide-therapeutics |
| Description | Universidade do Porto visit: Invited talk |
| Form Of Engagement Activity | Participation in an activity, workshop or similar |
| Part Of Official Scheme? | No |
| Geographic Reach | International |
| Primary Audience | Postgraduate students |
| Results and Impact | I was asked to provide an invited talk on my research "Peptide Hydrogel and Nanotubes for Biomaterial and Drug Delivery Applications" to other University academics, postgraduate and undergraduate researchers as part of a seminar series. |
| Year(s) Of Engagement Activity | 2023 |
| URL | https://www.i3s.up.pt/training-detail.php?v=283#:~:text=The%20course%20is%20designed%20for,doctoral%... |
| Description | YouTube video: Dr Garry Laverty - Peptide Hydrogel and Nanotubes for Biomaterial and Drug Delivery Applications |
| Form Of Engagement Activity | Engagement focused website, blog or social media channel |
| Part Of Official Scheme? | No |
| Geographic Reach | International |
| Primary Audience | Public/other audiences |
| Results and Impact | A YouTube webinar highlighting our research project was developed and posted on our School of Pharmacy Queen's University Belfast social media channels which has generated interest from potential PhD students and questions from industry and researchers in the drug delivery area. |
| Year(s) Of Engagement Activity | 2022 |
| URL | https://www.youtube.com/watch?v=BjEgxrQFa1g |
