Darshan R Telange, Pragati V Pandhare, Krutika R Sawarkar, Ujwala N Mahajan, Saurabh B Ganorkar, Amol S Warokar
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Nevertheless, its low oral bioavailability because of low water solubility, inadequate absorption, short half-life, and rapid clearance hampered its clinical applications.</p><p><strong>Objective: </strong>The study aimed to extract, isolate, characterize, and formulate the Phospholipon ®90H complex and evaluate for improved solubility, antiasthmatic and pharmacokinetic potential of CURs.</p><p><strong>Methods: </strong>Phospholipon®90H-based complex of curcuminoids (CPLC) was synthesized via solvent evaporation technique and reported an improvement of solubility, antiasthmatic, and pharmacokinetic potential of CURs. CPLC was physico-chemically and functionally evaluated by Fourier transforms infrared spectroscopy, differential scanning calorimetry, powder x-ray diffractometry, oral bioavailability, and antiasthmatic activity.</p><p><strong>Results: </strong>Ethyl acetate rhizome extracts (EARE) displayed ~17.42 % w/w extraction yield of CURs. CPLC revealed high entrapment of CURs (~ 92.55 % w/w) within the polar head of phospholipids. Small particle size ~ 194 nm with zeta potential value ~ -20.4 mV suggests the physical stability of CPLC. Physical analysis evidenced the formation of stable and amorphous CPLC by establishing hydrophobic and weak intermolecular forces between CURs and Phospholipon ®90H. Undoubtedly, the amorphous CPLC raised the aqueous solubility of CURs (~2-fold) compared to pure CURs. CPLC formulations (~ 20 mg/kg of CURs, p.o.) significantly lowered the leucocyte and eosinophil count compared to pure CURs. CPLC improved the oral bioavailability of CURs compared to pure CURs.</p><p><strong>Conclusion: </strong>Results highlight that CPLC could be established as a breakthrough respiratory nanocarrier for CURs and other phytocompounds with respiratory potential.</p>","PeriodicalId":10881,"journal":{"name":"Current pharmaceutical biotechnology","volume":" ","pages":""},"PeriodicalIF":2.2000,"publicationDate":"2024-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Extraction, Isolation, Characterization, and Development of Phospholipids Complex Nanocarrier for Improved Solubility, Antiasthmatic, and Pharmacokinetic Potential of Curcuminoids.\",\"authors\":\"Darshan R Telange, Pragati V Pandhare, Krutika R Sawarkar, Ujwala N Mahajan, Saurabh B Ganorkar, Amol S Warokar\",\"doi\":\"10.2174/0113892010326636240919094339\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Curcuma longa Linn. 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引用次数: 0
摘要
背景:姜黄(姜科)是一种药用植物,其姜黄素(CURs)具有显著的生物活性。然而,由于水溶性低、吸收不足、半衰期短、清除快等原因,其口服生物利用度较低,阻碍了其临床应用:本研究旨在提取、分离、表征和配制磷脂素 ®90H复合物,并评估其在改善 CURs 的溶解度、抗哮喘和药代动力学潜力方面的作用:方法:通过溶剂蒸发技术合成了以磷脂酰 ®90H为基础的姜黄素复合物(CPLC),并报道了该复合物改善了姜黄素的溶解性、抗哮喘性和药动学潜力。通过傅立叶变换红外光谱法、差示扫描量热法、粉末 X 射线衍射仪、口服生物利用度和抗哮喘活性对 CPLC 进行了物理化学和功能评价:醋酸乙酯根茎提取物(EARE)的 CURs 提取率约为 17.42%(重量百分比)。液相色谱(CPLC)显示,CURs(约 92.55 % w/w)在磷脂的极性头中有很高的吸附率。小粒径 ~ 194 nm,zeta 电位值 ~ -20.4 mV,这表明 CPLC 具有物理稳定性。物理分析表明,通过在 CURs 和磷脂 ®90H 之间建立疏水和微弱的分子间作用力,形成了稳定的无定形 CPLC。毫无疑问,与纯 CURs 相比,无定形 CPLC 提高了 CURs 的水溶性(约 2 倍)。与纯 CURs 相比,CPLC 制剂(约 20 毫克/千克 CURs,口服)显著降低了白细胞和嗜酸性粒细胞计数。与纯 CURs 相比,CPLC 提高了 CURs 的口服生物利用度:结论:研究结果表明,CPLC 可以作为一种突破性的呼吸道纳米载体,用于 CURs 和其他具有呼吸道潜力的植物化合物。
Extraction, Isolation, Characterization, and Development of Phospholipids Complex Nanocarrier for Improved Solubility, Antiasthmatic, and Pharmacokinetic Potential of Curcuminoids.
Background: Curcuma longa Linn. (Zingiberaceae) is a medicinal plant with significant biological activities owing to curcuminoids (CURs). Nevertheless, its low oral bioavailability because of low water solubility, inadequate absorption, short half-life, and rapid clearance hampered its clinical applications.
Objective: The study aimed to extract, isolate, characterize, and formulate the Phospholipon ®90H complex and evaluate for improved solubility, antiasthmatic and pharmacokinetic potential of CURs.
Methods: Phospholipon®90H-based complex of curcuminoids (CPLC) was synthesized via solvent evaporation technique and reported an improvement of solubility, antiasthmatic, and pharmacokinetic potential of CURs. CPLC was physico-chemically and functionally evaluated by Fourier transforms infrared spectroscopy, differential scanning calorimetry, powder x-ray diffractometry, oral bioavailability, and antiasthmatic activity.
Results: Ethyl acetate rhizome extracts (EARE) displayed ~17.42 % w/w extraction yield of CURs. CPLC revealed high entrapment of CURs (~ 92.55 % w/w) within the polar head of phospholipids. Small particle size ~ 194 nm with zeta potential value ~ -20.4 mV suggests the physical stability of CPLC. Physical analysis evidenced the formation of stable and amorphous CPLC by establishing hydrophobic and weak intermolecular forces between CURs and Phospholipon ®90H. Undoubtedly, the amorphous CPLC raised the aqueous solubility of CURs (~2-fold) compared to pure CURs. CPLC formulations (~ 20 mg/kg of CURs, p.o.) significantly lowered the leucocyte and eosinophil count compared to pure CURs. CPLC improved the oral bioavailability of CURs compared to pure CURs.
Conclusion: Results highlight that CPLC could be established as a breakthrough respiratory nanocarrier for CURs and other phytocompounds with respiratory potential.
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