Cited by 54Advancements in Transdermal Drug DeliveryAdvanced Drug Delivery SystemsNanoparticle-Based Drug Delivery

Polymer conjugated retinoids for controlled transdermal delivery

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Castleberry, Steven A., Quadir, Mohiuddin A., Sharkh, Malak Abu, Shopsowitz, Kevin E., Hammond, Paula T.·2017·Journal of Controlled Release

Abstract

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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Crossref · 10.1016/j.jconrel.2017.07.003

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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.”
  • 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.”

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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)
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
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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