Bifunctional Peptidomimetic Prodrugs of Didanosine for Improved Intestinal Permeability and Enhanced Acidic Stability: Synthesis, Transepithelial Transport, Chemical Stability and Pharmacokinetics

• Published in: Molecular pharmaceutics Vol. 8; no. 2; pp. 319 - 329
• Main Authors: Yan, Zhongtian, Sun, Jin, Chang, Yannan, Liu, Yanhua, Fu, Qiang, Xu, Youjun, Sun, Yongbing, Pu, Xiaohui, Zhang, Youxi, Jing, Yongkui, Yin, Shiliang, Zhu, Meng, Wang, Yongjun, He, Zhonggui
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 04.04.2011
• Subjects: Acids - chemistry; Administration, Oral; Animals; Biological Availability; Caco-2 Cells; Cell Membrane Permeability - drug effects; Didanosine - analogs & derivatives; Didanosine - chemical synthesis; Didanosine - chemistry; Didanosine - pharmacokinetics; Didanosine - pharmacology; Humans; Intestinal Absorption - drug effects; Intestines - drug effects; Liver - drug effects; Male; Peptidomimetics; Prodrugs - chemical synthesis; Prodrugs - pharmacokinetics; Prodrugs - pharmacology; Rats; Rats, Sprague-Dawley; Tissue Distribution; Transendothelial and Transepithelial Migration; Valine - analogs & derivatives; Valine - chemical synthesis; Valine - pharmacokinetics; Valine - pharmacology; prodrug; didanosine; peptide transporter; stability; permeability
• ISSN: 1543-8384; 1543-8392
• DOI: 10.1021/mp100376q

Five peptidomimetic prodrugs of didanosine (DDI) were synthesized and designed to improve bioavailability of DDI following oral administration via targeting intestinal oligopeptide transporter (PepT1) and enhancing chemical stability. The permeability of prodrugs was screened in Caco-2 cells grown on permeable supports. 5′-O-l-Valyl ester prodrug of DDI (compound 4a) demonstrated the highest membrane permeability and was selected as the optimal target prodrug for further studies. The uptake of glycylsarcosine (Gly-Sar, a typical substrate of PepT1) by Caco-2 cells could be inhibited by compound 4a in a concentration-dependent manner. The Caco-2 cells were treated with 0.2 nM leptin for enhanced PepT1 expression. The uptake of compound 4a was markedly increased in the leptin-treated Caco-2 cells compared with the control Caco-2 cells, both of which were obviously inhibited by 20 mM Gly-Sar. The K m and V max values of kinetic study of compound 4a transported by PepT1 in Caco-2 cells were 0.91 mM and 11.94 nmol/mg of protein/10 min, respectively. The chemical stability studies were performed in simulated gastric fluid (SGF), phosphate buffers under various pH conditions, rat tissue homogenates and plasma at 37 °C. The concentrations of DDI could not be detected in the two minutes in SGF. But compound 4a could significantly increase DDI acidic stability, and its t 1/2 was extended to as long as 36 min in SGF. Compound 4a was stable in pH 6.0 phosphate buffer but could be quickly transformed into DDI in plasma and tissue homogenates. The oral absolute bioavailability of DDI was 47.2% and 7.9% after compound 4a and DDI were orally administered to rats at a dose of 15 mg/kg, respectively. The coadministration with antiacid agent could also suggest that compound 4a was more stable under harsh acidic conditions compared with DDI. Compound 4a bioavailability in rats was reduced to 33.9% when orally coadministrated with Gly-Sar (100 mg/kg). The In Vivo bioactivation mechanism of compound 4a was investigated by comparing the levels of DDI and compound 4a in the jugular and portal veins in rats. The plasma concentration of intact compound 4a was very low in portal veins and could hardly be detected in the jugular vein. In conclusion, compound 4a could significantly improve the oral bioavailability of DDI in rats through PepT1-mediated absorption and enhanced acidic stability, followed by rapid and mostly intracellular bioactivation, the majority in the intestinal cells but the minority in the liver. Additionally, the prodrug strategy targeted to intestinal PepT1 could offer a promising strategy to improve oral bioavailability of poorly absorbed didanosine.