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Shell modulation by tailoring substituents in chitosan for LbL-assembled microcapsules

机译:通过为LbL组装的微胶囊定制壳聚糖中的取代基来调节壳

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摘要

By AFM we report the successful modulation of shell structure (morphology and shell thickness) of microcapsules through tailoring molecular substituents of chitosan. The shell thickness of hollow (HPCS/SA) n (n=5, 7, 9) capsules is more than 3 times that of the (QACS/SA) n (n=5, 7, 9) capsules, due to less charges carried by the neutral -NH _2 substituent group and the induced coily conformation in HPCS, while more charges carried by the positively charged -N(CH3)3+ substituent and the induced extended conformation in QACS (HPCS: hydroxyl propyl chitosan; QACS: quaternary ammonium chitosan; SA: sodium alginate). The ultrathin shells of microcapsules assembled in this work by the layer-by-layer (LbL) self-assembly technique rather than the traditional method of mixing CS, SA and CaCl _2 enable the thickness modulation characterization by AFM on the atomic scale. These microcapsules with tunable shell thickness provide important guidance for potential drug delivery and sustained release.
机译:通过原子力显微镜,我们报道了通过调整壳聚糖的分子取代基成功调节微胶囊的壳结构(形态和壳厚度)的方法。中空(HPCS / SA)n(n = 5、7、9)胶囊的壳厚度是(QACS / SA)n(n = 5、7、9)胶囊的壳厚的3倍以上,原因是电荷少在HPCS中由中性-NH _2取代基携带和诱导的螺旋构象,而在QACS中更多的带正电荷的-N(CH3)3+取代基和诱导的扩展构象(HPCS:羟丙基壳聚糖; QACS:季铵盐)壳聚糖铵; SA:藻酸钠)。通过逐层(LbL)自组装技术而不是传统的将CS,SA和CaCl _2混合的方法组装而成的微胶囊超薄壳,可以通过原子力显微镜(AFM)进行厚度调制表征。这些具有可调外壳厚度的微胶囊为潜在的药物输送和持续释放提供了重要的指导。

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