Nakanishi K, Masada M, Nadai T
Faculty of Pharmaceutical Sciences, Setsunan University, Osaka, Japan.
J Pharmacobiodyn. 1990 Dec;13(12):760-5. doi: 10.1248/bpb1978.13.760.
The influence of suppository bases and adjuvants on the release rate of drugs and the absorption of non-absorbable drugs such as sulfanilic acid (SA) and sulfaguanidine (SG), was investigated following the rectal administration of suppositories. The suppository bases used were lipophilic bases such as Witepsol W 35, H 15, S 55, E 75 and hydrophilic base such as macrogol. SA was rapidly released from macrogol, W 35, H 15 and S 55, except E 75. On the other hand, SG was rapidly released from macrogol, whereas the release of SG from lipophilic bases was slow. Rectal absorption of SA and SG following administration of each drug alone in suppository form was slight. On the addition of diclofenac sodium (DF) as absorption promoter the blood levels of SA and SG released from all suppositories increased by about two to four fold compared with those suppositories containing only SA or SG, respectively. However, the absorption of SG still did not attain sufficient levels by the administration of DF only. The rectal absorption of SG was markedly increased by the release rate of the drug from the suppository. These results indicate that after administration of these suppositories the bioavailability of non-absorbable drugs was sufficiently improved by enhancing both the release rate from the suppositories and the rectal membrane permeability.
在直肠给药栓剂后,研究了栓剂基质和辅料对药物释放速率以及对诸如磺胺酸(SA)和磺胺脒(SG)等难吸收药物吸收的影响。所用的栓剂基质为亲脂性基质,如Witepsol W 35、H 15、S 55、E 75,以及亲水性基质,如聚乙二醇。除E 75外,SA从聚乙二醇、W 35、H 15和S 55中快速释放。另一方面,SG从聚乙二醇中快速释放,而从亲脂性基质中释放缓慢。以栓剂形式单独给药每种药物后,SA和SG的直肠吸收轻微。加入双氯芬酸钠(DF)作为吸收促进剂后,与仅含SA或SG的栓剂相比,从所有栓剂中释放的SA和SG的血药浓度分别增加了约两到四倍。然而,仅通过DF给药,SG的吸收仍未达到足够水平。SG的直肠吸收因药物从栓剂中的释放速率而显著增加。这些结果表明,在给予这些栓剂后,通过提高栓剂的释放速率和直肠膜通透性,难吸收药物的生物利用度得到了充分改善。