首页> 外文期刊>International Journal of Nanomedicine >Core-shell hybrid liposomal vesicles loaded with panax notoginsenoside: preparation, characterization and protective effects on global cerebral ischemia/reperfusion injury and acute myocardial ischemia in rats
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Core-shell hybrid liposomal vesicles loaded with panax notoginsenoside: preparation, characterization and protective effects on global cerebral ischemia/reperfusion injury and acute myocardial ischemia in rats

机译:三七总皂甙核壳混合脂质体囊泡:对大鼠全脑缺血/再灌注损伤和急性心肌缺血的制备,表征和保护作用

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Purpose: Novel panax notoginsenoside-loaded core-shell hybrid liposomal vesicles (PNS-HLV) were developed to resolve the restricted bioavailability of PNS and to enhance its protective effects in vivo on oral administration.Methods: Physicochemical characterizations of PNS-HLV included assessment of morphology, particle size and zeta potential, encapsulation efficiency (EE%), stability and in vitro release study. In addition, to evaluate its oral treatment potential, we compared the effect of PNS-HLV on global cerebral ischemia/reperfusion and acute myocardial ischemia injury with those of PNS solution, conventional PNS-loaded nanoparticles, and liposomes.Results: In comparison with PNS solution, conventional PNS-loaded nanoparticles and liposomes, PNS-HLV was stable for at least 12 months at 4°C. Satisfactory improvements in the EE% of notoginsenoside R1, ginsenoside Rb1, and ginsenoside Rg1 were shown with the differences in EE% shortened and the greater controlled drug release profiles were exhibited from PNS-HLV. The improvements in the physicochemical properties of HLV contributed to the results that PNS-HLV was able to significantly inhibit the edema of brain and reduce the infarct volume, while it could markedly inhibit H2O2, modified Dixon agar, and serum lactate dehydrogenase, and increase superoxide dismutase (P < 0.05).Conclusion: The results of the present study imply that HLV has promising prospects for improving free drug bioactivity on oral administration.
机译:目的:开发新型三七总皂苷核壳混合脂质体囊泡(PNS-HLV)以解决PNS受限制的生物利用度并增强其对口服的体内保护作用。方法:PNS-HLV的理化特性包括评估形态,粒度和Zeta电位,包封效率(EE%),稳定性和体外释放研究。此外,为了评估其口服治疗的潜力,我们比较了PNS-HLV与PNS溶液,常规PNS负载的纳米颗粒和脂质体对全脑缺血/再灌注和急性心肌缺血的影响。结果:与PNS进行比较溶液,常规的装有PNS的纳米颗粒和脂质体,PNS-HLV在4°C稳定至少12个月。三七皂苷R1,人参皂苷Rb1和人参皂苷Rg1的EE%令人满意地改善,EE%的差异缩短,PNS-HLV表现出更大的药物控制释放曲线。 HLV的理化性质的改善有助于以下结果:PNS-HLV能够显着抑制脑水肿并减少梗塞体积,同时可以显着抑制H2O2,修饰的Dixon琼脂和血清乳酸脱氢酶,并增加超氧化物歧化酶结论:本研究结果表明HLV可以改善口服给药的游离药物生物活性。

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