Kohri N - Search Results

1

The use of an in vitro dissolution and absorption system to evaluate oral absorption of two weak bases in pH-independent controlled-release formulations.

Sugawara M, Kadomura S, He X, Takekuma Y, Kohri N, Miyazaki K. Sugawara M, et al. Among authors: kohri n. Eur J Pharm Sci. 2005 Sep;26(1):1-8. doi: 10.1016/j.ejps.2005.02.017. Eur J Pharm Sci. 2005. PMID: 15961297

2

Sustained release of nifedipine from granules.

Kohri N, Mori K, Miyazaki K, Arita T. Kohri N, et al. J Pharm Sci. 1986 Jan;75(1):57-61. doi: 10.1002/jps.2600750113. J Pharm Sci. 1986. PMID: 3958907

3

Improving the oral bioavailability of albendazole in rabbits by the solid dispersion technique.

Kohri N, Yamayoshi Y, Xin H, Iseki K, Sato N, Todo S, Miyazaki K. Kohri N, et al. J Pharm Pharmacol. 1999 Feb;51(2):159-64. doi: 10.1211/0022357991772277. J Pharm Pharmacol. 1999. PMID: 10217314

4

Improvement of dissolution and bioavailability for mebendazole, an agent for human echinococcosis, by preparing solid dispersion with polyethylene glycol.

Chiba Y, Kohri N, Iseki K, Miyazaki K. Chiba Y, et al. Among authors: kohri n. Chem Pharm Bull (Tokyo). 1991 Aug;39(8):2158-60. doi: 10.1248/cpb.39.2158. Chem Pharm Bull (Tokyo). 1991. PMID: 1797442

5

Improving the oral bioavailability of sulpiride by a gastric-retained form in rabbits.

Kohri N, Naasani I, Iseki K, Miyazaki K. Kohri N, et al. J Pharm Pharmacol. 1996 Apr;48(4):371-4. doi: 10.1111/j.2042-7158.1996.tb05935.x. J Pharm Pharmacol. 1996. PMID: 8794985

6

Purification by ceftibuten-affinity chromatography and the functional reconstitution of oligopeptide transporter(s) in rat intestinal brush-border membrane.

Iseki K, Yonemura K, Kikuchi T, Naasani I, Sugawara M, Kobayashi M, Kohri N, Miyazaki K. Iseki K, et al. Among authors: kohri n. Biochim Biophys Acta. 1998 Mar 6;1370(1):161-8. doi: 10.1016/s0005-2736(97)00258-7. Biochim Biophys Acta. 1998. PMID: 9518592 Free article.

7

Improving the oral bioavailability of sulpiride by sodium oleate in rabbits.

Naasani I, Kohri N, Iseki K, Miyazaki K. Naasani I, et al. Among authors: kohri n. J Pharm Pharmacol. 1995 Jun;47(6):469-73. doi: 10.1111/j.2042-7158.1995.tb05833.x. J Pharm Pharmacol. 1995. PMID: 7674129

8

Purification and liposomal reconstitution of the oligopeptide transport activity in rat renal cortex using ceftibuten-affinity chromatography.

Iseki K, Naasani I, Kikuchi T, Sugawara M, Kobayashi M, Kohri N, Miyazaki K. Iseki K, et al. Among authors: kohri n. Biochim Biophys Acta. 1998 Jan 19;1368(2):329-37. doi: 10.1016/s0005-2736(97)00201-0. Biochim Biophys Acta. 1998. PMID: 9459609 Free article.

9

Release characteristics of nifedipine sustained-release granules in vitro and in healthy subjects.

Kohri N, Miyazaki K, Arita T, Shimono H, Nomura A, Yasuda H. Kohri N, et al. Chem Pharm Bull (Tokyo). 1987 Jun;35(6):2504-9. doi: 10.1248/cpb.35.2504. Chem Pharm Bull (Tokyo). 1987. PMID: 3664846 No abstract available.

10

A simple method for the simulation of unbound serum disopyramide concentration in patients.

Kishino S, Kohri N, Iseki K, Miyazaki K, Nomura A, Yasuda H. Kishino S, et al. Among authors: kohri n. J Pharmacobiodyn. 1991 Sep;14(9):493-9. doi: 10.1248/bpb1978.14.493. J Pharmacobiodyn. 1991. PMID: 1779403

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