Jacob Joby, Sukumaran Nimisha Pulikkal, Jude Shintu
R&D Centre, Aurea Biolabs (P) Ltd., Kolenchery, 682311 Kerala, India.
ACS Omega. 2021 Feb 17;6(8):5560-5568. doi: 10.1021/acsomega.0c05963. eCollection 2021 Mar 2.
l-ascorbic acid (AA) or vitamin C is a crucial nutrient needed for optimal health. However, being unable to be synthesized by the body, it is thus necessary to be included in health care products. Moreover, AA is one of the antioxidants that occur naturally, which is used in pharmaceutical and food products as an antioxidant additive. However, AA is vulnerable to environmental settings and undergoes oxidative degradation to dehydroascorbic acid and further to inactive products. Therefore, new research strategies and approaches are required to augment its stability. The objective of this study is to develop and characterize a fiber-reinforced-phospholipid (FRP) matrix-based vehicle, Zeal-AA, for the delivery of AA and optimize the oral bioavailability of the obtained AA powder using an efficacy study by open-label, randomized, single-dose, two-treatment, two-sequence, two-period, two-way crossover. The structural and surface morphologies were analyzed by Fourier transform infrared spectroscopy, transmission electron microscopy, scanning electron microscopy, and differential scanning calorimetry studies. Encapsulation efficiency, mean particle size, size distribution, ζ-potential measurements, and ADMET profiling revealed the potential delivery system for AA. AUC was found to be 55.23 (mg/dL) for Zeal-AA, whereas it was 9.38 (mg/dL) for AA, and was found to be 6.69 (mg/dL) for Zeal-AA, whereas it was 1.23 (mg/dL) for AA, with a fold difference of bioavailability in terms of AUC found to be 5.9 fold. The results show that a single oral dose of Zeal-AA is capable of rising the AA levels in the body relative to the control up to 24 h.
l-抗坏血酸(AA)或维生素C是维持最佳健康状态所需的关键营养素。然而,由于人体无法合成它,因此有必要将其纳入保健品中。此外,AA是天然存在的抗氧化剂之一,在药品和食品中用作抗氧化剂添加剂。然而,AA易受环境影响,会氧化降解为脱氢抗坏血酸,并进一步转化为无活性产物。因此,需要新的研究策略和方法来提高其稳定性。本研究的目的是开发并表征一种基于纤维增强磷脂(FRP)基质的载体Zeal-AA,用于递送AA,并通过开放标签、随机、单剂量、双治疗、双序列、双周期、双向交叉的疗效研究优化所得AA粉末的口服生物利用度。通过傅里叶变换红外光谱、透射电子显微镜、扫描电子显微镜和差示扫描量热法研究分析了其结构和表面形态。包封效率、平均粒径、粒径分布、ζ电位测量和ADMET分析揭示了AA的潜在递送系统。发现Zeal-AA的AUC为55.23(mg/dL),而AA的AUC为9.38(mg/dL);发现Zeal-AA的 为6.69(mg/dL),而AA的 为1.23(mg/dL),就AUC而言,生物利用度的倍数差异为5.9倍。结果表明,单次口服Zeal-AA能够使体内AA水平相对于对照组在长达24小时内升高。