Polymer conjugated retinoids for controlled transdermal delivery
Open accessAbstract
All-trans retinoic acid (ATRA), a derivative of vitamin A, is a common component in cosmetics and commercial acne creams as well as being a first-line chemotherapeutic agent. Today, formulations for the topical application of ATRA rely on creams and emulsions to incorporate the highly hydrophobic ATRA drug. These strategies, when applied to the skin, deliver ATRA as a single bolus, which is immediately taken up into the skin and contributes to many of the known adverse side effects of ATRA treatment, including skin irritation and hair loss. Herein we present a new concept in topical delivery of retinoids by covalently bonding the drug through a hydrolytically degradable ester linkage to a common hydrophilic polymer, polyvinyl alcohol (PVA), creating an amphiphilic nanomaterial that is water-soluble. This PVA bound ATRA can then act as a pro-drug and accumulate within the skin to allow for the sustained controlled delivery of active ATRA. This approach was demonstrated to release active ATRA out to 10days in vitro while significantly enhancing dermal accumulation of the ATRA in explant pig skin. In vivo we demonstrate that the pro-drug formulation reduces application site inflammation compared to free ATRA and retains the drug at the application site at measurable quantities for up to six days.
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In chemical interaction, RA is typically conjugated chemically to one of the components of the nanoparticle by biodegradable ester, amide, or disulfide linkages.
“Concerning chemical interaction, RA is typically conjugated chemically to one of the components of the nanoparticle by biodegradable ester50,52, amide26,53–55, or disulfide56 linkages.”
From Advances and challenges in retinoid delivery systems in regenerative and therapeutic medicine (2020) · cites this paper as [52]
Several RA-polymer conjugates have been developed to release RA by hydrolytic cleavage of ester bonds, by enzymatic cleavage of amide bonds by proteases present in the targeted tissue, or by reducing environments such as the cell cytoplasm.
“For example, several RA-polymer conjugates have been developed to release RA by hydrolytic cleavage of ester bonds50,52, by enzymatic cleavage of amide bonds by proteases present in the targeted tissue28,65–67 or by reducing environments56 such as the cell cytoplasm.”
From Advances and challenges in retinoid delivery systems in regenerative and therapeutic medicine (2020) · cites this paper as [52]
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References 54 · Cited by 54
- Authors
- Castleberry, S. A., Quadir, M. A., Sharkh, M. A., Shopsowitz, K. E., & Hammond, P. T.
- Affiliations
- Harvard–MIT Division of Health Sciences and Technology (US)
- Koch Institute for Integrative Cancer Research At MIT (US)
- Massachusetts Institute of Technology (US)
- Institute for Soldier Nanotechnologies (US)
- Corresponding author
- Hammond, Paula T.
- Venue
- Journal of Controlled Release
- Publisher
- Elsevier BV
- Published
- 2017-09
- Volume
- 262
- Pages
- 1-9
- ISSN
- 0168-3659 (ISSN-L)
- PMC
- PMC5641977
- OpenAlex
- W2727726868
- Cited by
- 54
- References
- 54
- Citations by year
- 2026: 2 · 2025: 5 · 2024: 4 · 2023: 4 · 2022: 10 · 2021: 8 · 2020: 8 · 2019: 7 · 2018: 5
- FWCI
- 2.83
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (am, 319 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Journal of Controlled Release (acceptedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- DSpace@MIT (Massachusetts Institute of Technology) (submittedVersion, cc-by-nc-nd)
- PMC
- Funders
- U.S. Army (W911NF-07-D-0004)
- NCI (2P30CA014051-39)
- Topics
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advancements in Transdermal Drug Delivery
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Keywords
- all-trans retinoic acid, retinoids, transdermal drug delivery, polymer conjugates, polyvinyl alcohol, prodrugs, sustained drug release, topical formulation, acne treatment, skin irritation
- MeSH terms
- Administration, Cutaneous, Animals, Cell Survival, Delayed-Action Preparations, Female, Polyvinyl Alcohol, Prodrugs, Skin, Swine, Tretinoin, NIH 3T3 Cells, Nanostructures, Mice, Drug Liberation
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