不同溶剂提取法评价马来西亚余甘子体外抗尿石性

M. Gul, N. Muhammad, A. Pauzi, M. Bakar, B. Talip, N. Abdullah, N. Rahim, Wan Nur Ain Syukriah, Wan Nur Ain Syukriah Wan Marzuki, L. Din, N. Ibrahim
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引用次数: 2

摘要

在马来西亚,千余子传统上用于治疗肾脏疾病和尿路结石。因此,本研究旨在通过测定草酸钙(CaOx)晶体的溶出率和CaOx的聚集率,来评价不同溶剂(正己烷、乙酸乙酯、甲醇和水)提取液对体外抗尿石性能的影响。以赛石为阳性对照。用分光光度法考察了半胱氨酸对CaOx的成核、聚集斜率和生长的影响。甲醇的产率最高,为5.74%。甲醇对CaOx晶体聚集的抑制作用最大(66.67%±1.61),主要由生物碱、甾体、萜类和单宁组成。对草酸钙晶体的溶出效果表明,水合提物对CaOx的溶出效果为63.33%±1.44。P. niruri显著(P < 0.05)抑制了CaOx结晶成核和聚集的斜率,降低了结晶密度。本研究的结果证实了乌桕叶可作为尿石症的治疗介质。然而,需要进一步的研究来分离和鉴定有效成分及其在体内的证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of Phyllanthus niruri L. from Malaysia for In-vitro Anti-Urolithiatic Properties by Different Solvent Extraction
The Phyllanthus niruri is traditionally used for curing of kidney disorders and urinary stones in Malaysia. Hence the current work was aimed to evaluate the effect of different solvents extract (n- hexane, ethyl acetate, methanol and water) of P. niruri for in vitro anti-urolithiatic properties in terms of inhibition activity on CaOx by using the rate of CaOx aggregation assay and dissolution of calcium oxalate (CaOx) crystal by using titrimetry method. Cystone was used as positive control. The effects of cystone on slope of nucleation and aggregation as well as growth of CaOx were evaluated spectrophotometrically. The highest yield percentage of P.niruri was occupied by methanol (5.74 %). The maximum inhibition against aggregation of CaOx crystals was also occupied by methanol (66.67 % ± 1.61) and was comprised with alkaloid, steroid, terpenoid and tannin. Dissolution effect on calcium oxalate crystals indicates that the aqueous extracts of P. niruri was found to be more effective in dissolution of CaOx with 63.33 %   ± 1.44. P. niruri significantly (P < 0.05) inhibited the slope of nucleation and aggregation of CaOx crystallization, and reduced the crystal density. The results of the present study confirmed that P. niruri leaves can be used as remedial mediator for urolithiasis. However, further studies are required for isolation and identification of active constituents and their in-vivo confirmation.
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