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https://www.sciencedirect.com/science/article/pii/S0927776511002797
Oct 01, 2011 · Chitosan-cyclodextrin nanospheres were prepared by in situ formation through Michael addition between N-maleated chitosan (NMC) and per-6-thio-β-cyclodextrin sodium salt in an aqueous medium. This facile preparation method did not involve any organic solvent and surfactant. Through adjusting the preparation conditions, the nanospheres with a relatively narrow size distribution could …Author: Jun Wang, Jing-Yi Zong, Dong Zhao, Ren-Xi Zhuo, Si-Xue Cheng
https://www.researchgate.net/publication/51200756_In_situ_formation_of_chitosan-cyclodextrin_nanospheres_for_drug_delivery
Chitosan-cyclodextrin nanospheres were prepared by in situ formation through Michael addition between N-maleated chitosan (NMC) and per-6-thio-β-cyclodextrin sodium salt in an aqueous medium.
https://www.deepdyve.com/lp/elsevier/in-situ-formation-of-chitosan-cyclodextrin-nanospheres-for-drug-tkRx3b2FU6
Oct 01, 2011 · Read "In situ formation of chitosan-cyclodextrin nanospheres for drug delivery, Colloids and Surfaces B: Biointerfaces" on DeepDyve, the largest online rental service for scholarly research with thousands of academic publications available at your fingertips.
https://www.sciencedirect.com/science/article/pii/S0939641112001038
Within the past 20 years, a considerable amount of work has been published on chitosan and its potential use in drug delivery systems. In contrast to all other polysaccharides having a monograph in a pharmacopeia, chitosan has a cationic character because of its primary amino groups.Author: Andreas Bernkop-Schnürch, Sarah Dünnhaupt
https://www.researchgate.net/scientific-contributions/2031805507_Jun_Wang
Chitosan-cyclodextrin nanospheres were prepared by in situ formation through Michael addition between N-maleated chitosan (NMC) and per-6-thio-β-cyclodextrin sodium salt in an aqueous medium.
https://journals.sagepub.com/doi/abs/10.1177/0885328216651183
Delivery of amphiphobic drugs (insoluble in both water and oil) has been a great challenge in drug delivery. SNX-2112, a novel inhibitor of Hsp90, is a promising drug candidate for treating various types of cancers; however, the insolubility greatly limits its clinical application.Author: Lixia Zheng, Shao Wu, Li Tan, Huo Tan, Baodan Yu
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