Comparison of Serum 25-Hydroxyvitamin D Levels After A Single Oral Dose of Vitamin D3 Formulations in Mild Vitamin D3 Deficiency

IF 0.4 Q4 PHARMACOLOGY & PHARMACY Journal of Pharmacology & Pharmacotherapeutics Pub Date : 2021-10-01 DOI:10.4103/jpp.jpp_105_21
Kavita Munjal, Sourabh Sharma, Shallu Sharma, Deepak Kumar, Ajay Choudhary, R. Berwal, Ashok Kumar
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引用次数: 1

Abstract

Objective: To compare the levels of serum 25 Hydroxyvitamin D levels after a single large oral dose (60,000 IU) of different vitamin D3 formulations. Materials and Methods: Ninety-one volunteers with mild vitamin D deficiency (18–29 ng/ml) were selected and randomly assigned to three parallel groups. Groups-I received liquid, Group-II received sachet, and Group-III received tablet formulation of cholecalciferol as a single dose of 60,000 IU orally after 8–10 h of overnight fasting. Serum 25(OH) D concentrations were measured at baseline, 24 h, 7 days, and 14 days after drug administration. Various hematology and biochemical parameters were also assessed for baseline safety evaluation. Results: Baseline serum 25(OH) D concentrations in Groups I (liquid), II (sachet), and III (tablet) was 24.75 ± 4.77 ng/mL, 23.25 ± 4.15 ng/mL, and 23.18 ± 5.52 ng/mL, respectively. After supplemented with three formulations, only tablet group after 24 h showed increase in serum 25-OH-D concentration of 8.07 units from its baseline. Whereas after 7th day, no significant difference in absorption was observed but after 14th day, all three groups showed increase in serum 25-OH-D concentration, in which tablet group (50.10 ± 94.99 ng/ml) showed highest increase in absorption (26.92 units) from their baseline values. During intergroup comparison between three formulations at the time of investigation, only liquid group after 24 h showed increased serum concentration by P values (0.03, 0.02) as compared to sachet and tablet group. However, After 7th and 14th day, there was no statistically difference was observed between three groups. Conclusion: Single oral dose of 60,000 IU dose of vitamin D liquid formulation has higher absorption value as after 24 h and tablet formulation showed higher absorption after 7th days. In emergency paucity of vitamin D, these observations findings can have critical conclusions to state the suitable dietary formulation of vitamin D.
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轻度维生素D3缺乏患者单次口服维生素D3制剂后血清25-羟基维生素D水平的比较
目的:比较不同维生素D3制剂单次大剂量口服(60000 IU)后血清25羟基维生素D水平。材料与方法:选择91名轻度维生素D缺乏症(18-29 ng/ml)的志愿者,随机分为3个平行组。1组给予液体,2组给予小袋,3组给予胆钙化醇片剂,空腹8-10小时,单剂量60000 IU口服。在给药后基线、24小时、7天和14天测定血清25(OH) D浓度。各种血液学和生化参数也被评估为基线安全性评价。结果:ⅰ组(液体)、ⅱ组(小袋)、ⅲ组(片剂)血清25(OH) D基线浓度分别为24.75±4.77 ng/mL、23.25±4.15 ng/mL、23.18±5.52 ng/mL。添加3种制剂后,24 h后仅片剂组血清25-OH-D浓度较基线升高8.07单位。第7天时,3组血清25-OH-D浓度均升高,其中片剂组(50.10±94.99 ng/ml)较基线值增加最多(26.92单位)。在调查时三种剂型的组间比较中,只有液体组在24 h后血清浓度较小香囊和片剂组升高P值(0.03,0.02)。第7、14天时,三组间差异无统计学意义。结论:60000 IU剂量的维生素D液体制剂单次口服在24 h后具有较高的吸收值,片剂在7 D后具有较高的吸收值。在紧急缺乏维生素D的情况下,这些观察结果可以得出关键结论,说明维生素D的适当膳食配方。
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