Fabrication of Dissolving Polymer Microneedles for Controlled Drug Encapsulation and Delivery: Bubble and Pedestal Microneedle Designs

被引:205
作者
Chu, Leonard Y. [1 ]
Choi, Seong-O [2 ,3 ]
Prausnitz, Mark R. [1 ,3 ]
机构
[1] Georgia Inst Technol, Wallace Coulter Dept Biomed Engn, Atlanta, GA 30332 USA
[2] Georgia Inst Technol, Sch Elect & Comp Engn, Atlanta, GA 30332 USA
[3] Georgia Inst Technol, Sch Chem & Biomol Engn, Atlanta, GA 30332 USA
基金
美国国家卫生研究院;
关键词
transdermal drug delivery; dissolving microneedles; microneedle fabrication; drug encapsulation; skin; ARRAY PATCH SYSTEM; TRANSDERMAL DELIVERY; PENETRATION ENHANCERS; COATED MICRONEEDLES; VACCINE; IMMUNIZATION; SKIN; TRANSPORT;
D O I
10.1002/jps.22140
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Dissolving microneedle patches offer promise as a simple, minimally invasive method of drug and vaccine delivery to the skin that avoids the need for hypodermic needles. However, it can be difficult to control the amount and localization of drug within microneedles. In this study, we developed novel microneedle designs to improve control of drug encapsulation and delivery using dissolving microneedles by (i) localizing drug in the microneedle tip, (ii) increasing the amount of drug loaded in microneedles while minimizing wastage, and (iii) inserting microneeclles more fully into the skin. Localization of our model drug, sulforhodamine B in the microneedle tip by either casting a highly concentrated polymer solution as the needle matrix or incorporating an air bubble at the base of the microneedle achieved approximately 80% delivery within 10 mm compared to 20% delivery achieved by the microneedles encapsulating nonlocalized drug. As another approach, a pedestal was introduced to elevate each microneedle for more complete insertion into the skin and to increase its drug loading capacity by threefold from 0.018 to 0.053 mu L per needle. Altogether, these novel microneedle designs provide a new set of tools to fabricate dissolving polymer microneedles with improved control over drug encapsulation, loading, and delivery. (C) 2010 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 99:4228-4238, 2010
引用
收藏
页码:4228 / 4238
页数:11
相关论文
共 32 条
[1]  
[Anonymous], MODIFIED RELEASE DRU
[2]   Micro-scale devices for transdermal drug delivery [J].
Arora, Anubhav ;
Prausnitz, Mark R. ;
Mitragotri, Samir .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2008, 364 (02) :227-236
[3]   Microfabricated silicon microneedles for nonviral cutaneous gene delivery [J].
Chabri, F ;
Bouris, K ;
Jones, T ;
Barrow, D ;
Hann, A ;
Allender, C ;
Brain, K ;
Birchall, J .
BRITISH JOURNAL OF DERMATOLOGY, 2004, 150 (05) :869-877
[4]  
Choi S.O., 2006, SOL STAT SENS ACT MI
[5]   Transdermal delivery of desmopressin using a coated microneedle array patch system [J].
Cormier, M ;
Johnson, B ;
Ameri, M ;
Nyam, K ;
Libiran, L ;
Zhang, DD ;
Daddona, P .
JOURNAL OF CONTROLLED RELEASE, 2004, 97 (03) :503-511
[6]   Transdermal drug delivery by coated microneedles: Geometry effects on effective skin thickness and drug permeability [J].
Davidson, Adam ;
Al-Qallaf, Barrak ;
Das, Diganta Bhusan .
CHEMICAL ENGINEERING RESEARCH & DESIGN, 2008, 86 (11A) :1196-1206
[7]   Silicon micromachined hollow microneedles for transdermal liquid transport [J].
Gardeniers, HJGE ;
Luttge, R ;
Berenschot, EJW ;
de Boer, MJ ;
Yeshurun, SY ;
Hefetz, M ;
van't Oever, R ;
van den Berg, A .
JOURNAL OF MICROELECTROMECHANICAL SYSTEMS, 2003, 12 (06) :855-862
[8]   Effect of microneedle design on pain in human volunteers [J].
Gill, Harvinder S. ;
Denson, Donald D. ;
Burris, Brett A. ;
Prausnitz, Mark R. .
CLINICAL JOURNAL OF PAIN, 2008, 24 (07) :585-594
[9]   Coated microneedles for transdermal delivery [J].
Gill, Harvinder S. ;
Prausnitz, Mark R. .
JOURNAL OF CONTROLLED RELEASE, 2007, 117 (02) :227-237
[10]   Transcutaneous immunization: A human vaccine delivery strategy using a patch [J].
Glenn, GM ;
Taylor, DN ;
Li, XR ;
Frankel, S ;
Montemarano, A ;
Alving, CR .
NATURE MEDICINE, 2000, 6 (12) :1403-1406