Characterization of norfloxacine release from tablet coated with a new pH-sensitive polymer, P-4135F

被引:25
作者
Hu, ZP [1 ]
Shimokawa, T [1 ]
Ohno, T [1 ]
Kimura, G [1 ]
Mawatari, SS [1 ]
Kamitsuna, M [1 ]
Yoshikawa, Y [1 ]
Masuda, S [1 ]
Takada, K [1 ]
机构
[1] Kyoto Pharmaceut Univ, Dept Pharmacokinet, Yamashina Ku, Kyoto 6078414, Japan
关键词
colon delivery; pH-sensitive polymer; P-4135F; norfloxacine; first-appearance rime in blood; rats; beagle dogs;
D O I
10.3109/10611869909085505
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
A new pH-sensitive polymer, P-4135F, was evaluated as a colon delivery device for norfloxacine (NFLX) which is used for the therapy of patients with Vero toxin-producing Escherichia coli gastroenteritis. P-4135F has a dissolution threshold pH of 7.2 which is higher than the conventional pH-sensitive polymers, Eudragit S100 and L100, To compare the dissolution site of P-4135F coated tablets with other enteric polymer coatings, mini-tablets containing sodium fluorescein (FL) as a model drug were prepared by coating them with the three polymers. After oral administration of FL mini-tablets to rats, the: first-appearance time, T-i, of FL into the systemic circulation was measured, The T(i)s were 0.7 +/- 0.2 h for Eudragit L100, 1.8 +/- 0.4 h for S100 and 2.0 +/- 0.3 h for P-4135F. Direct inspection of the dissolution process of the FL mini-tablets after oral administration to rats was performed by abdominal incision studies. All of the coated FL mini-tablets started to dissolve in the rat ileum. The dissolution sites were identified to be proximal to the ileocecal junction for P-4135F, at the middle part of the ileum for Eudragit S100 and at the proximal part of the ileum for Eudragit L100. NFLX tablets with different membrane thicknesses of P-4135F were prepared and were orally administered to beagle dogs. The colon delivery efficiency was evaluated by measuring the T-i of NFLX into the systemic circulation. The mean T(i)s were 1.33 +/- 0.33 h for 56.8 +/- 0.5 mu m membranes, 3.75 +/- 0.25 h for 64.6 +/- 0.7 mu m membranes, 4.00 +/- 1.00 h for 70.5 +/- 0.5 mu m membranes and 3.00 +/- 1.00 h for 74.9 +/- 0.4 mu m membranes, Bq comparing the T-i, 4.33 +/- 0.33 h, obtained after oral administration of NFLX in a pressure-controlled colon delivery capsule, and the colon arrival time, 3.5 +/- 0.3 h, determined by a sulfasalazine test in beagle dogs, P-4135F coated NFLX tablets appeared to dissolve and disintegrate before reaching the colon. Studies using rats and beagle dogs have suggested that P-4135F dissolves in the lower part of the small intestine, i.e., the ileum. These studies also suggest that this new polymer will be useful for the delivery of NFLX to the lower part of the small intestine.
引用
收藏
页码:223 / 232
页数:10
相关论文
共 27 条
[1]   A PHASE-I STUDY OF CHEMICALLY SYNTHESIZED VEROTOXIN (SHIGA-LIKE TOXIN) PK-TRISACCHARIDE RECEPTORS ATTACHED TO CHROMOSORB FOR PREVENTING HEMOLYTIC-UREMIC SYNDROME [J].
ARMSTRONG, GD ;
ROWE, PC ;
GOODYER, P ;
ORRBINE, E ;
KLASSEN, TP ;
WELLS, G ;
MACKENZIE, A ;
LIOR, H ;
BLANCHARD, C ;
AUCLAIR, F ;
THOMPSON, B ;
RAFTER, DJ ;
MCLAINE, PN .
JOURNAL OF INFECTIOUS DISEASES, 1995, 171 (04) :1042-1045
[2]  
David A, 1997, STP PHARMA SCI, V7, P546
[3]  
EVANS DF, 1986, GUT, V16, P185
[4]  
GAZZANIGA A, 1995, STP PHARMA SCI, V5, P83
[5]   ORAL DELAYED-RELEASE SYSTEM FOR COLONIC SPECIFIC DELIVERY [J].
GAZZANIGA, A ;
IAMARTINO, P ;
MAFFIONE, G ;
SANGALLI, ME .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1994, 108 (01) :77-83
[6]  
HARDY JG, 1989, DRUG DELIVERY GASTRO
[7]   Scintigraphic evaluation of a new capsule-type colon specific drug delivery system in healthy volunteers [J].
Ishibashi, T ;
Pitcairn, GR ;
Yoshino, H ;
Mizobe, M ;
Wilding, IR .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1998, 87 (05) :531-535
[8]   Design and evaluation of a new capsule-type dosage form for colon-targeted delivery of drugs [J].
Ishibashi, T ;
Hatano, H ;
Kobayashi, M ;
Mizobe, M ;
Yoshino, H .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1998, 168 (01) :31-40
[9]   COMPARISON OF THE GASTROINTESTINAL ANATOMY, PHYSIOLOGY, AND BIOCHEMISTRY OF HUMANS AND COMMONLY USED LABORATORY-ANIMALS [J].
KARARLI, TT .
BIOPHARMACEUTICS & DRUG DISPOSITION, 1995, 16 (05) :351-380
[10]   SPORADIC CASES OF HEMOLYTIC-UREMIC SYNDROME ASSOCIATED WITH FECAL CYTO-TOXIN AND CYTOTOXIN-PRODUCING ESCHERICHIA-COLI IN STOOLS [J].
KARMALI, MA ;
PETRIC, M ;
STEELE, BT ;
LIM, C .
LANCET, 1983, 1 (8325) :619-620