Evaluation of poly(lactic-co-glycolic acid) and poly(DL-lactide-co-ε-caprolactone) electrospun fibers for the treatment of HSV-2 infection
Creators
- 1. Department of Bioengineering, University of Louisville, Louisville, KY 40202 (United States)
- 2. Department of Pharmacology and Toxicology, University of Louisville, Louisville, KY 40202 (United States)
- 3. Center for Predictive Medicine, University of Louisville, Louisville, KY 40202 (United States)
- 4. Department of Medicine, University of Louisville, Louisville, KY 40202 (United States)
- 5. Department of Microbiology and Immunology, University of Louisville, Louisville, KY 40202 (United States)
Description
More diverse multipurpose prevention technologies are urgently needed to provide localized, topical pre-exposure prophylaxis against sexually transmitted infections (STIs). In this work, we established the foundation for a multipurpose platform, in the form of polymeric electrospun fibers (EFs), to physicochemically treat herpes simplex virus 2 (HSV-2) infection. To initiate this study, we fabricated different formulations of poly(lactic-co-glycolic acid) (PLGA) and poly(DL-lactide-co-ε-caprolactone) (PLCL) EFs that encapsulate Acyclovir (ACV), to treat HSV-2 infection in vitro. Our goals were to assess the release and efficacy differences provided by these two different biodegradable polymers, and to determine how differing concentrations of ACV affected fiber efficacy against HSV-2 infection and the safety of each platform in vitro. Each formulation of PLGA and PLCL EFs exhibited high encapsulation efficiency of ACV, sustained-delivery of ACV through one month, and in vitro biocompatibility at the highest doses of EFs tested. Additionally, all EF formulations provided complete and efficacious protection against HSV-2 infection in vitro, regardless of the timeframe of collected fiber eluates tested. This work demonstrates the potential for PLGA and PLCL EFs as delivery platforms against HSV-2, and indicates that these delivery vehicles may be expanded upon to provide protection against other sexually transmitted infections. - Highlights: • PLGA and PLCL EFs exhibit sustained-delivery of ACV through one month. • EFs exhibit high ACV encapsulation efficiency and in vitro biocompatibility. • EFs serve as both physical and chemical barriers to HSV-2 infection. • Potent in vitro efficacy is provided against HSV-2 infection for all formulations. • HSV-2 protection is independent of administration times within one month.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.msec.2016.11.029Additional details
Identifiers
- DOI
- 10.1016/j.msec.2016.11.029;
- PII
- S0928-4931(16)32108-7;
Publishing Information
- Journal Title
- Materials Science and Engineering. C, Biomimetic Materials, Sensors and Systems
- Journal Volume
- 72
- Journal Page Range
- p. 238-251
- ISSN
- 0928-4931
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 49040192
- Subject category
- S60: APPLIED LIFE SCIENCES; S36: MATERIALS SCIENCE;
- Descriptors DEI
- BIODEGRADATION; CONCENTRATION RATIO; DRUG DELIVERY; DRUGS; EFFICIENCY; ENCAPSULATION; FIBERS; GLYCOLIC ACID; HERPES SIMPLEX; IN VITRO; POLYMERS; PREVENTIVE MEDICINE; VIRUSES
- Descriptors DEC
- CARBOXYLIC ACIDS; CHEMICAL REACTIONS; DECOMPOSITION; DIMENSIONLESS NUMBERS; DISEASES; HYDROXY ACIDS; INFECTIOUS DISEASES; MEDICINE; MICROORGANISMS; MONOCARBOXYLIC ACIDS; ORGANIC ACIDS; ORGANIC COMPOUNDS; PARASITES; SKIN DISEASES; VIRAL DISEASES
Optional Information
- Copyright
- Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.