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健康成年人生物利用度/生物等效性研究中药物/药品所接触的回肠末端和盲肠内容物的特征

Characterization of Contents of Distal Ileum and Cecum to Which Drugs/Drug Products are Exposed During Bioavailability/Bioequivalence Studies in Healthy Adults.

作者信息

Reppas Christos, Karatza Eleni, Goumas Constantinos, Markopoulos Constantinos, Vertzoni Maria

机构信息

Faculty of Pharmacy, School of Health Sciences, National & Kapodistrian University of Athens, Panepistimiopolis, 157 71, Zografou, Greece.

Red Cross Hospital of Athens, Athens, Greece.

出版信息

Pharm Res. 2015 Oct;32(10):3338-49. doi: 10.1007/s11095-015-1710-6. Epub 2015 May 22.

Abstract

PURPOSE

Characterize the contents of distal ileum and cecum in healthy adults under conditions simulating the bioavailability/bioequivelance studies of drug products in fasted and fed state.

METHODS

Twelve males participated in a two-phase crossover study. Phase I: subjects remained fasted overnight plus 4.5 h in the morning prior to colonoscopy. Phase II: subjects remained fasted overnight, consumed breakfast in the morning, and abstain from food until colonoscopy, 4.5 h after breakfast. Upon sampling, volume, pH and buffer capacity were measured; after ultracentrifugation, supernatant was physicochemically characterized and non-liquid particles diameter was measured.

RESULTS

In distal ileum, pH is 8.1 and size of non-liquid particles is ~200 μm, regardless of dosing conditions; in fed state, liquid fraction was lower whereas osmolality and carbohydrate content were higher. In cecum, the environment was similar with previously characterized environment in the ascending colon; in fasted state, size of non-liquid particles is smaller than in distal ileum (70 μm). Fluid composition in distal ileum is different from cecum, especially in fasted state.

CONCLUSION

Differences in luminal environment between distal ileum and cecum may impact the performance of orally administered products which deliver drug during residence in lower intestine. Dosing conditions affect cecal environment more than in distal ileum.

摘要

目的

在模拟药物产品在空腹和进食状态下的生物利用度/生物等效性研究的条件下,表征健康成年人回肠末端和盲肠的内容物。

方法

12名男性参与了一项两阶段交叉研究。第一阶段:受试者在结肠镜检查前禁食过夜加上午4.5小时。第二阶段:受试者禁食过夜,早上吃早餐,然后在早餐后4.5小时结肠镜检查前禁食。取样时,测量体积、pH值和缓冲容量;超速离心后,对上清液进行物理化学表征并测量非液体颗粒直径。

结果

在回肠末端,无论给药条件如何,pH值约为8.1,非液体颗粒大小约为200μm;在进食状态下,液体部分较低,而渗透压和碳水化合物含量较高。在盲肠中,环境与先前表征的升结肠环境相似;在空腹状态下,非液体颗粒大小比回肠末端小(约70μm)。回肠末端的液体成分与盲肠不同,尤其是在空腹状态下。

结论

回肠末端和盲肠管腔环境的差异可能会影响在小肠下段停留期间释放药物的口服产品的性能。给药条件对盲肠环境的影响大于回肠末端。

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