Chitosan Microneedle Patches for Sustained Transdermal Delivery of Macromolecules

• Published in: Biomacromolecules Vol. 13; no. 12; pp. 4022 - 4031
• Main Authors: Chen, Mei-Chin, Ling, Ming-Hung, Lai, Kuan-Ying, Pramudityo, Esar
• Format: Journal Article
• Language: English
• Published: Washington, DC American Chemical Society 10.12.2012
• Subjects: Administration, Cutaneous; Animals; Applied sciences; Biocompatible Materials - chemistry; Biological and medical sciences; Chitosan - chemistry; Drug Delivery Systems - instrumentation; Drug Delivery Systems - methods; Exact sciences and technology; General pharmacology; Macromolecular Substances - chemistry; Male; Medical sciences; Microinjections - methods; Natural polymers; Needles; Pharmaceutical technology. Pharmaceutical industry; Pharmacology. Drug treatments; Physicochemistry of polymers; Rats; Rats, Sprague-Dawley; Serum Albumin, Bovine - chemistry; Skin - drug effects; Skin - metabolism; Starch and polysaccharides; Swine; Pyramidal shape; Transdermal system; Rat; Control release polymer; Rodentia; Mechanical properties; Drug carrier; Serum albumin; Experimental study; In vitro; Protein; In vivo; Vertebrata; Mammalia; Animal; Morphology; Oside polymer; Chitosan; Kinetics; Manufacturing; Patch; Release; Microneedle
• ISSN: 1525-7797; 1526-4602
• DOI: 10.1021/bm301293d

This paper introduces a chitosan microneedle patch for efficient and sustained transdermal delivery of hydrophilic macromolecules. Chitosan microneedles have sufficient mechanical strength to be inserted in vitro into porcine skin at approximately 250 μm in depth and in vivo into rat skin at approximately 200 μm in depth. Bovine serum albumin (BSA, MW = 66.5 kDa) was used as a model protein to explore the potential use of chitosan microneedles as a transdermal delivery device for protein drugs. In vitro drug release showed that chitosan microneedles can provide a sustained release of BSA for at least 8 days (approximately 95% of drugs released in 8 days). When the Alexa Fluor 488-labeled BSA (Alexa 488-BSA)-loaded microneedles were applied to the rat skin in vivo, confocal microscopic images showed that BSA can gradually diffuse from the puncture sites to the dermal layer and the fluorescence of Alexa 488-BSA can be observed at the depth of 300 μm. In addition, encapsulation of BSA within the microneedle matrix did not alter the secondary structure of BSA, indicating that the gentle nature of the fabrication process allowed for encapsulation of fragile biomolecules. These results suggested that the developed chitosan microneedles may serve as a promising device for transdermal delivery of macromolecules in a sustained manner.