Degradability of chitosan micro/nanoparticles for pulmonary drug delivery

被引:176
|
作者
Islam, Nazrul [1 ,2 ]
Dmour, Isra [3 ]
Taha, Mutasem O. [4 ]
机构
[1] Queensland Univ Technol, Fac Hlth, Sch Clin Sci, Pharm Discipline, Brisbane, Qld 4000, Australia
[2] QUT, Inst Hlth & Biomed Innovat, 60 Musk Ave, Brisbane, Qld 4059, Australia
[3] Al Ahliyya Amman Univ, Fac Pharm & Med Sci, Amman, Jordan
[4] Univ Jordan, Fac Pharm, Dept Pharmaceut Sci, Amman 11942, Jordan
关键词
Analytical chemistry; Bioengineering; Biogeoscience; Biomedical engineering; Cancer research; Infectious disease; Materials chemistry; Nanotechnology; Pharmaceutical chemistry; Physical chemistry; IN-VIVO DEGRADATION; CONTROLLED-RELEASE; MOLECULAR-WEIGHT; CROSS-LINKING; NANOPARTICLES FORMULATION; GLUTARALDEHYDE; LYSOZYME; CHITIN; POWDER; VITRO;
D O I
10.1016/j.heliyon.2019.e01684
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Chitosan, a natural carbohydrate polymer, has long been investigated for drug delivery and medical applications due to its biodegradability, biocompatibility and low toxicity. The micro/nanoparticulate forms of chitosan are reported to enhance the efficiency of drug delivery with better physicochemical properties including improved solubility and bioavailability. This polymer is known to be biodegradable and biocompatible; however, cross-linked chitosan particles may not be biodegradable. Crosslinkers (e.g., tripolyphosphate and glutaraldehyde) are needed for efficient micro/nanoparticle formation, but it is not clear whether the resultant particles are biodegradable or able to release the encapsulated drug fully. To date, no studies have conclusively demonstrated the complete biodegradation or elimination of chitosan nanoparticles in vivo. Herein we review the synthesis and degradation mechanisms of chitosan micro/nanoparticles frequently used in drug delivery especially in pulmonary drug delivery to understand whether these nanoparticles are biodegradable.
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页数:9
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