Delivery of multipurpose prevention drug combinations from electrospun nanofibers using composite microarchitectures

被引:62
作者
Blakney, Anna K. [1 ]
Krogstad, Emily A. [1 ]
Jiang, Yonghou H. [1 ]
Woodrow, Kim A. [1 ]
机构
[1] Univ Washington, Dept Bioengn, Seattle, WA 98195 USA
基金
美国国家科学基金会;
关键词
co-delivery; electrospinning; antiretroviral; contraceptive; microbicide; multipurpose prevention technology; IMMUNODEFICIENCY-VIRUS TYPE-1; FUSION INHIBITOR T-20; HIV; INFECTIONS; RELEASE; FIBERS; CONTRACEPTIVES; MATS;
D O I
10.2147/IJN.S61664
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Background: Electrospun drug-eluting fabrics have enormous potential for the delivery of physicochemically diverse drugs in combination by controlling the underlying material chemistry and fabric microarchitecture. However, the rationale for formulating drugs at high drug loading in the same or separate fibers is unknown but has important implications for product development and clinical applications. Methods: Using a production-scale free-surface electrospinning instrument, we produced electrospun nanofibers with different microscale geometries for the co-delivery of tenofovir (TFV) and levonorgestrel (LNG) - two lead drug candidates for multipurpose prevention of HIV acquisition and unintended pregnancy. We investigated the in vitro drug release of TFV and LNG combinations from composites that deliver the two drugs from the same fiber ( combined fibers) or from separate fibers in a stacked or interwoven architecture. For stacked composites, we also examined the role that fabric thickness has on drug-release - kinetics. We also measured the cytotoxicity and antiviral activity of the drugs delivered alone and in combination. Results: Herein, we report on the solution and processing parameters for the free-surface electrospinning of medical fabrics with controlled microarchitecture and high drug loading ( up to 20 wt%). We observed that in vitro release of the highly water-soluble TFV, but not the water-insoluble LNG, was affected by composite microarchitecture, fabric thickness, and drug content. Finally, we showed that the drug-loaded nanofibers are noncytotoxic and that the antiviral activity of TFV is preserved through the electrospinning process and when combined with LNG. Conclusion: Electrospun fabrics with high drug loading create multicomponent systems that benefit from the independent control of the nanofibrous microarchitecture. Our findings are significant because they will inform the design and production of composite electrospun fabrics for the co-delivery of physicochemically diverse drugs that may be useful for multipurpose prevention.
引用
收藏
页码:2967 / 2978
页数:12
相关论文
共 33 条
[1]   Optimised Anaesthesia to Reduce Post Operative Cognitive Decline (POCD) in Older Patients Undergoing Elective Surgery, a Randomised Controlled Trial [J].
Ballard, Clive ;
Jones, Emma ;
Gauge, Nathan ;
Aarsland, Dag ;
Nilsen, Odd Bjarte ;
Saxby, Brian K. ;
Lowery, David ;
Corbett, Anne ;
Wesnes, Keith ;
Katsaiti, Eirini ;
Arden, James ;
Amaoko, Derek ;
Prophet, Nicholas ;
Purushothaman, Balaji ;
Green, David .
PLOS ONE, 2012, 7 (06)
[2]   Novel biodegradable sandwich-structured nanofibrous drug-eluting membranes for repair of infected wounds: an in vitro and in vivo study [J].
Chen, Dave Wei-Chih ;
Liao, Jun-Yi ;
Liu, Shih-Jung ;
Chan, Err-Cheng .
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2012, 7 :763-771
[3]   Effective use of hormonal contraceptives Part II: combined hormonal injectables, progestogen-only injectables and contraceptive implants [J].
Chrisman, CE ;
Curtis, KM ;
Mohllajee, AP ;
Gaffield, ME ;
Peterson, HB .
CONTRACEPTION, 2006, 73 (02) :125-133
[4]   The mechanisms of drug release from solid dispersions in water-soluble polymers [J].
Craig, DQM .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 231 (02) :131-144
[5]   Acyclic nucleoside phosphonates: Past, present and future - Bridging chemistry to HIV, HBV, HCV, HPV, adeno-, herpes-, and poxvirus infections: The phosphonate bridge [J].
De Clercq, E. .
BIOCHEMICAL PHARMACOLOGY, 2007, 73 (07) :911-922
[6]   Sensitivity of human immunodeficiency virus type 1 to the fusion inhibitor T-20 is modulated by coreceptor specificity defined by the V3 loop of gp120 [J].
Derdeyn, CA ;
Decker, JM ;
Sfakianos, JN ;
Wu, XY ;
O'Brien, WA ;
Ratner, L ;
Kappes, JC ;
Shaw, GM ;
Hunter, E .
JOURNAL OF VIROLOGY, 2000, 74 (18) :8358-8367
[7]   Preparation and characterization of injectable microspheres of contraceptive hormones [J].
Dhanaraju, MD ;
Vema, K ;
Jayakumar, R ;
Vamsadhara, C .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2003, 268 (1-2) :23-29
[8]   Combining prevention of HIV-1, other sexually transmitted infections and unintended pregnancies: Development of dual-protection technologies [J].
Friend, David R. ;
Doncel, Gustavo F. .
ANTIVIRAL RESEARCH, 2010, 88 :S47-S54
[9]   Twenty micrograms vs. >20 μg estrogen oral contraceptives for contraception:: systematic review of randomized controlled trials [J].
Gallo, MF ;
Nanda, K ;
Grimes, DA ;
Schulz, KF .
CONTRACEPTION, 2005, 71 (03) :162-169
[10]   Electrospun fibers for tissue engineering, drug delivery, and wound dressing [J].
Goh, Yi-Fan ;
Shakir, Imran ;
Hussain, Rafaqat .
JOURNAL OF MATERIALS SCIENCE, 2013, 48 (08) :3027-3054