环糊精
PLGA公司
化学
差示扫描量热法
强力霉素
药理学
植入
体内
体外
核化学
色谱法
抗生素
生物化学
外科
医学
热力学
物理
生物技术
生物
作者
Elham Khodaverdi,Farhad Eisvand,Mohammad Sina Nezami,Seyedeh Nesa Rezaeian Shiadeh,Hossein Kamali,Farzin Hadizadeh
出处
期刊:Current Drug Delivery
[Bentham Science]
日期:2021-09-20
卷期号:18 (6): 729-740
被引量:5
标识
DOI:10.2174/1567201817999201103195104
摘要
Doxycycline (DOX) is used in treating a bacterial infection, especially for periodontitis treatment.To reduce irritation of DOX for subgingival administration and increase the chemical stability and against enzymatic, the complex of α-cyclodextrin with DOX was prepared and loaded into injectable in situ forming implant based on PLGA.FTIR, molecular docking studies, X-ray diffraction, and differential scanning calorimetry was performed to characterize the DOX/α-cyclodextrin complex. Finally, the in-vitro drug release and modeling, morphological properties, and cellular cytotoxic effects were also evaluated.The stability of DOX was improved with complex than pure DOX. The main advantage of the complex is the almost complete release (96.31 ± 2.56 %) of the drug within 14 days of the implant, whereas in the formulation containing the pure DOX and the physical mixture the DOX with α-cyclodextrin release is reached to 70.18 ± 3.61 % and 77.03 ± 3.56 %, respectively. This trend is due to elevate of DOX stability in the DOX/ α-cyclodextrin complex form within PLGA implant that confirmed by the results of stability.Our results were indicative that the formulation containing DOX/α-cyclodextrin complex was biocompatible and sustained-release with minimum initial burst release.
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