Evaluation of poly(lactic-co-glycolic acid) and poly(DL-lactide-co-ε-caprolactone) electrospun fibers for the treatment of HSV-2 infection

被引:26
作者
Aniagyei, Stella E. [1 ]
Sims, Lee B. [1 ]
Malik, Danial A. [3 ]
Tyo, Kevin M. [3 ,5 ]
Curry, Keegan C. [1 ]
Kim, Woihwan [2 ]
Hodge, Daniel A. [1 ]
Duan, Jinghua [1 ,5 ]
Steinbach-Rankins, Jill M. [1 ,3 ,4 ,5 ]
机构
[1] Univ Louisville, Dept Bioengn, Louisville, KY 40202 USA
[2] Univ Louisville, Dept Med, Louisville, KY 40202 USA
[3] Univ Louisville, Dept Pharmacol & Toxicol, Louisville, KY 40202 USA
[4] Univ Louisville, Dept Microbiol & Immunol, Louisville, KY 40202 USA
[5] Univ Louisville, Ctr Predict Med, Louisville, KY 40202 USA
来源
MATERIALS SCIENCE AND ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2017年 / 72卷
关键词
Electrospun fibers; Herpes simplex virus 2 (HSV-2); Sexually transmitted infections (STIs); Microbicide; Antiviral; Acyclovir; Intravaginal; Drug delivery systems; TENOFOVIR DISOPROXIL FUMARATE; SIMPLEX-VIRUS TYPE-2; SEXUALLY-TRANSMITTED INFECTIONS; HERPES-SIMPLEX; DRUG-DELIVERY; DUAL PROTECTION; UNINTENDED PREGNANCY; TUNABLE RELEASE; 14-DAY SAFETY; HIV;
D O I
10.1016/j.msec.2016.11.029
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
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-coglycolic acid) (PLGA) and poly(m-lactide-co-epsilon-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. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:238 / 251
页数:14
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