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使用Plackett-Burman析因设计筛选离子交联壳聚糖-三聚磷酸钠微球用于治疗袋内感染。

Screening of ionically crosslinked chitosan-tripolyphosphate microspheres using Plackett-Burman factorial design for the treatment of intrapocket infections.

作者信息

Yadav Sarita Kumari, Khan Gayasuddin, Bansal Monika, Vardhan Harsh, Mishra Brahmeshwar

机构信息

a Department of Pharmaceutics , Indian Institute of Technology, Banaras Hindu University , Varanasi , Uttar Pradesh , India.

b Department of Pharmacy , Moti Lal Nehru Medical College , Allahabad , Uttar Pradesh , India.

出版信息

Drug Dev Ind Pharm. 2017 Nov;43(11):1801-1816. doi: 10.1080/03639045.2017.1349782. Epub 2017 Jul 24.

Abstract

OBJECTIVE

Application of Plackett-Burman factorial design to investigate the effect of processing factors in the fabrication of ionically crosslinked chitosan-tripolyphosphate (CS-TPP) microspheres.

SIGNIFICANCE

Microspheres were screened and optimized to provide maximum process yield (PY), encapsulation efficiency (EE), and time for 80% drug release (T) and minimum burst and particles size (PS), for successful application in periodontitis.

METHODS

Processing factors viz. method of preparation (MOP), CS, TPP, crosslinking time (CT), agitation (AS), and drying technique (DT) were selected. Solid state characterization was performed by Fourier-Transform infrared (FTIR), differential scanning calorimetry (DSC), X-ray diffraction (XRD), and scanning electron microscopy (SEM). Mucoadhesion, cytocompatibility, and stability of microspheres were also evaluated.

RESULTS

Pareto analysis and analysis of variance, screened most significantly (p < .05) impacting process factors on selected responses. The optimized microspheres demonstrated: o/w emulsification method, CS (2.5%), TPP (5%), CT (120 min), AS (2000 rpm), and DT (freeze-dried), and provided PY- 95.67%, PS- 168.45%, EEOZ- 85.56%, EEDX- 91.34%, BOZ- 15.26%, BDX- 12.91%, TOZ- 47.09 and TDX- 67.95 minutes. FTIR illustrated compatibility between excipients and complexation of CS and TPP. XRD and DSC showed loss of crystallinity of entrapped drugs in microspheres. Biphasic drug release was observed for four days with non-Fickian kinetics. Furthermore, microspheres exhibited good mucoadhesivity (82.51%), antimicrobial activity against Staphylococcus aureus and Escherichia coli, cytocompatibility for L929 cells, and long-term stability.

CONCLUSIONS

Therefore, CS-TPP microspheres were found mucoadhesive, safe, stable and provided controlled and prolonged release of drugs. These properties confirmed its high potential and applicability in chronic periodontitis.

摘要

目的

应用Plackett-Burman析因设计研究离子交联壳聚糖-三聚磷酸钠(CS-TPP)微球制备过程中各工艺因素的影响。

意义

筛选并优化微球,以获得最大的工艺产率(PY)、包封率(EE)和80%药物释放时间(T),并使突释和粒径(PS)最小,从而成功应用于牙周炎治疗。

方法

选择制备方法(MOP)、壳聚糖(CS)、三聚磷酸钠(TPP)、交联时间(CT)、搅拌(AS)和干燥技术(DT)等工艺因素。通过傅里叶变换红外光谱(FTIR)、差示扫描量热法(DSC)、X射线衍射(XRD)和扫描电子显微镜(SEM)进行固态表征。还评估了微球的黏膜黏附性、细胞相容性和稳定性。

结果

帕累托分析和方差分析筛选出对所选响应影响最显著(p < 0.05)的工艺因素。优化后的微球表现为:水包油乳化法、CS(2.5%)、TPP(5%)、CT(120分钟)、AS(2000转/分钟)和DT(冷冻干燥),工艺产率为95.67%、粒径为168.45、初始包封率为85.56%、最终包封率为91.34%、初始突释为15.26%、最终突释为12.91%、初始80%药物释放时间为47.09分钟、最终80%药物释放时间为67.95分钟。FTIR表明辅料之间的相容性以及CS和TPP的络合。XRD和DSC显示微球中包封药物的结晶度丧失。观察到药物在四天内呈双相释放,具有非菲克动力学特征。此外,微球表现出良好的黏膜黏附性(82.51%)、对金黄色葡萄球菌和大肠杆菌的抗菌活性、对L929细胞的细胞相容性以及长期稳定性。

结论

因此,发现CS-TPP微球具有黏膜黏附性、安全性、稳定性,并能实现药物的控释和缓释。这些特性证实了其在慢性牙周炎中的高潜力和适用性。

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