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Pre-Formulation Study for Palatable Microbeads of Lycopene

机译:番茄红素可口微珠的预配制研究

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Lycopene is a widely used nutraceuticals for its antioxidant property but the molecule has poor aqueous solubility, high instability, and extremely low intestinal permeability leading to its poor bioavailability. In the present study, pre-formulation study was carried out to prepare sodium alginate microbeads with the intention to deliver an effective amount of lycopene for high absorption through oral route. A thorough physical characterization and spectral analysis were done to understand the characteristic of lycopene such as its melting point, UV spectrophotometric analysis, chromatography through reverse phase HPLC. Fourier transform infrared spectroscopy and differential scanning calorimetry were adopted to know the interaction of sodium alginate with lycopene. Box-Behnken design (version 9.0.2.0, Stat Ease Inc, USA) was used to analyse the effect of formulation variables such as sodium alginate (%), glutaraldehyde (%) and stirring speed on lycopene entrapment and its loading into microbeads. The adopted preformulation strategy revealed that lycopene was a crystalline powder with a sharp melting point at 155supo/supC and the prominent functional groups were present in the sample. UV and HPLC analysis revealed precise quantitation and authenticity of lycopene. Excipient compatibility also revealed inertness of sodium alginate. Response surface morphology revealed significant effect of alginate, glutaraldehyde and stirring speed on formation of best composition. Therefore, it is concluded that lycopene can be formulated as microbeads for oral drug delivery.
机译:番茄红素因其抗氧化性能而被广泛使用,但该分子的水溶性差,不稳定性高,肠通透性极低,从而导致其生物利用度差。在本研究中,进行了制剂前研究,以制备藻酸钠微珠,目的是通过口服途径递送有效量的番茄红素以高吸收。进行了彻底的物理表征和光谱分析,以了解番茄红素的特征,例如其熔点,紫外分光光度法分析,通过反相HPLC进行色谱分析。采用傅里叶变换红外光谱和差示扫描量热法了解藻酸钠与番茄红素的相互作用。使用Box-Behnken设计(版本9.0.2.0,美国Stat Ease Inc.)分析诸如海藻酸钠(%),戊二醛(%)和搅拌速度等配方变量对番茄红素截留及其装入微珠的影响。所采用的预配制策略表明番茄红素是一种结晶粉末,其熔点为155℃,具有明显的熔点,并且样品中存在明显的官能团。紫外和HPLC分析揭示了番茄红素的精确定量和真实性。赋形剂的相容性还显示出藻酸钠的惰性。响应表面形态显示藻酸盐,戊二醛和搅拌速度对最佳组合物形成有显着影响。因此,可以得出结论,番茄红素可以配制成用于口服药物递送的微珠。

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