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The Evaluation of Feasibility on Modified Chitosan as Transdermal Drug Delivery Enhancer and Tissue Engineering Scaffold
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本研究利用褐藻酸鈉與兩性幾丁聚醣交聯的水凝膠應用在藥物促滲劑和組織工程。實驗利用FT-IR和1H NMR確認其化學特性，其中冷凍乾燥的交聯支架利用SEM和拉力測試評估其應用在組織工程的可能性。根據SEM結果顯示，孔洞直徑約100~250 μm。
幾丁聚醣利用疏水性官能基 - 月桂酸和棕櫚酸完成架接，並評估此凝膠當做親水性藥物 - 間-苯二酚載體的經皮滲透效果。在體外經皮滲透實驗，利用垂直式經皮滲透儀進行監測並利用數學模型得知有效滲透係數。實驗配方分別為不加入幾丁聚醣的溶液為控制組，加入N-palmitoyl chitosan (PNC), N-lauryl chitosan (LNC), N-palmitoyl chitosan- alginate (PNC-A), N-lauryl chitosan- alginate (LNC-A)為比較組。根據結果，LNC具有當作藥物經皮滲透載體的潛力。|
Being the major contributor of permeation resistance of transdermal drug delivery system（TDDS）,stratum corneum (SC) has been the focus of TDDS research aiming at improving the efficiency of drug permeation through skin. One of the approaches toward that is to modify the physicochemical properties of the drug and thus alter the interaction between drug molecules and SC. Chitosan has received interest for medical and pharmaceutical applications due to its intrinsic properties including biocompatibility, biodegradability and non-antigenicity. In this work hydrogel solutions composed of cross-linked amphiphilic chitosan and alginate porous scaffold were prepared for the in vitro permeation experiments and tissue engineering. Experiments performed on the crosslinked scaffolds that physical properties were examined by SEM,and Tensile test（Young’s modulus）,as well as its chemical identity was determined by FT-IR and confirmed by 1H NMR. The morphology results showed the pore size ranged from 100 to 250 μm. The purpose of this study is to evaluate the transdermal permeation enhancement of the modification of the water-soluble chitosan with pendant hydrophobic groups to achieve non-covalent cross-linking with fatty acid, and as well evaluate the potential of the amphiphilic hydrogels as topical delivery carrier for the hydrophilic model compound Resorcinol (Re). Results were analyzed with a numerical model to produce quantitative indexes for the evaluation of transdermal drug delivery efficiency. A family of chitosan derivatives including N-palmitoyl chitosan (PNC), N-lauryl chitosan (LNC), N-palmitoyl chitosan- alginate (PNC-A), N-lauryl chitosan- alginate (LNC-A) were employed as permeation enhancers. The results suggested LNC was a significant enhancer for transdermal permeation of Re.
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