首页|乳铁蛋白修饰的纳米凝胶滴丸的制备及药物转运入脑性研究

乳铁蛋白修饰的纳米凝胶滴丸的制备及药物转运入脑性研究

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目的 改善天然药物的水溶性及将其转运入脑的效率,构建可负载难溶性药物的乳铁蛋白修饰的纳米凝胶滴丸剂并探究制备工艺,为神经退行性疾病的药物开发提供参考。方法 以难溶性药物淫羊藿苷为负载药物,利用反相微乳法制备乳铁蛋白修饰的海藻酸锌纳米凝胶,采用HPLC法测定纳米凝胶中淫羊藿苷的载药率和包封率。以圆整度、丸重差异和溶散时限为评价指标,采用单因素和Box-Behnken响应面法优选滴丸的最佳制备工艺,并采用傅里叶变换红外光谱分析表征,转篮法探究滴丸中纳米凝胶的释放行为,荧光示踪法比较滴丸药物舌下含服和口服的入脑效率。结果 HPLC法测得纳米凝胶的载药率为(2。67±0。05)%,包封率为(84。74±0。03)%。乳铁蛋白修饰的纳米凝胶滴丸的最佳制备工艺为:基质与纳米凝胶的比例 5∶1,滴距 5。5 cm,冷凝温度8。5℃。以修饰物乳铁蛋白为标志物,纳米凝胶体外累积释放率达到 92。25%。荧光示踪研究表明,与口服给药相比,滴丸通过舌下给药时,能更快、更有效地协助药物穿过血脑屏障进入脑内,提升了制剂将药物转运入脑的效率。结论 所制备的乳铁蛋白修饰的纳米凝胶可作为难溶性药物的负载平台,改善药物水溶性,进一步制备成滴丸剂舌下含服后极大提升了药物转运入脑的效率,提高了神经退行性患者的用药依从性,满足了临床用药需求。
Preparation of lactoferrin modified nanogel dropping pills and study on drug transport into brain
Objective To improve the water solubility of natural drugs and the efficiency of their transport into the brain,to prepare nanogel dropping pills modified with lactoferrin for loading poorly soluble drugs and investigate the preparation process,and to provide a reference for drug development in the field of neurodegenerative diseases.Methods Using the insoluble drug icariin as the payload,the lactoferrin-modified zinc alginate nanogels were prepared by the reverse-phase microemulsion method.The drug loading and encapsulation rates of icariin in the nanogel were determined by HPLC.Taking the utilizing parameters such as roundness,weight difference and disintegration time as evaluation indicators,the best preparation process of dropping pills was optimized by single factor experiments and Box-Behnken response surface methodology.It was characterized by Fourier transform infrared spectroscopy,the release behavior of nanogel in dropping pills was explored by basket rotating method,and the brain entry efficiency between sublingual and oral administration of drip pills were compared by fluorescence tracing method.Results The drug loading rate of the nanogel was(2.67±0.05)%,and the encapsulation rate was(84.74±0.03)%by HPLC.The optimal preparation process for lactoferrin modified nanogel dropping pills was as follows:the ratio of matrix to nano gel was 5:1,the drop distance was 5.5 cm,and the condensation temperature was 8.5℃.Using the modified lactoferrin as a marker,its cumulative release rate in vitro reached 92.25%.Fluorescence tracing studies showed that compared to the oral group,sublingual administration of dripping pills facilitated the faster and more effective passage of drugs through the blood-brain barrier,significantly enhanced the efficiency of drug transport into the brain.Conclusion The prepared lactoferrin-modified nanogels can be used as a loading platform for poorly soluble drugs and enhance the drug solubility.When further formulated into dripping pills,it significantly enhances the efficiency of drug transport into the brain after sublingual administration.This also enhances medication compliance among neurodegenerative patients and fulfills the clinical demand for the drug.

NanogelLactoferrinDropping pillsBox-Behnken response surface methodSublingual administrationNeurodegenerative disease

董勤唯、栗俏俏、崔元璐、陈昳冰

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天津中医药大学中医药研究院组分中药国家重点实验室(天津 301617)

现代中医药海河实验室(天津 301617)

纳米凝胶 乳铁蛋白 滴丸 Box-Behnken响应面法 舌下含服 神经退行性疾病

国家自然科学基金青年科学基金

82104399

2024

中国药师
国家药品监督管理局高级研修学院,武汉医药(集团)股份有限公司

中国药师

CSTPCD
影响因子:0.944
ISSN:1008-049X
年,卷(期):2024.27(5)
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