A study of prostatic tissue levels of latamoxef, cefoperazone and cefotaxime

Although Cephem antibiotics are transferred to the prostatic fluid in relatively low levels, they are clinically effective for bacterial prostatitis. In the present study, the prostatic tissue concentration of Latamoxef (LMOX), Cefoperazone (CPZ) and Cefotaxime (CTX) were determined, and their penet...

Description complète

Détails bibliographiques
Publié dans:Hinyokika kiyo. Acta urologica Japonica. - 1962. - 32(1986), 12 vom: 30. Dez., Seite 1831-41
Auteur principal: Takeuchi, N (Auteur)
Autres auteurs: Kinukawa, T, Matsuura, O, Hattori, R, Hasegawa, S, Ohshima, S, Ono, Y
Format: Article
Langue:Japanese
Publié: 1986
Accès à la collection:Hinyokika kiyo. Acta urologica Japonica
Sujets:English Abstract Journal Article Cefoperazone 7U75I1278D Cefotaxime N2GI8B1GK7 Moxalactam VUF6C936Z3
LEADER 01000caa a22002652c 4500
001 NLM024165573
003 DE-627
005 20250125185320.0
007 tu
008 231221s1986 xx ||||| 00| ||jpn c
028 5 2 |a pubmed25n0081.xml 
035 |a (DE-627)NLM024165573 
035 |a (NLM)2435132 
040 |a DE-627  |b ger  |c DE-627  |e rakwb 
041 |a jpn 
100 1 |a Takeuchi, N  |e verfasserin  |4 aut 
245 1 2 |a A study of prostatic tissue levels of latamoxef, cefoperazone and cefotaxime 
264 1 |c 1986 
336 |a Text  |b txt  |2 rdacontent 
337 |a ohne Hilfsmittel zu benutzen  |b n  |2 rdamedia 
338 |a Band  |b nc  |2 rdacarrier 
500 |a Date Completed 06.04.1987 
500 |a Date Revised 21.11.2013 
500 |a published: Print 
500 |a Citation Status MEDLINE 
520 |a Although Cephem antibiotics are transferred to the prostatic fluid in relatively low levels, they are clinically effective for bacterial prostatitis. In the present study, the prostatic tissue concentration of Latamoxef (LMOX), Cefoperazone (CPZ) and Cefotaxime (CTX) were determined, and their penetration rates into the prostatic tissue were analyzed. Before the transurethral resection of the prostate (TUR-P), 2 g of LMOX (21 patients), 1 g of CPZ (15 patients) and 2 g of CTX (14 patients) were intravenously administered in a total of 50 patients with benign prostatic hypertrophy at our two Hospitals. The prostatic tissue was taken by TUR-P at 30 minutes and 60 minutes after the injection. The serum concentration and the prostatic tissue concentration of the three antibiotics were determined by the bioassay method. Additionally their serum concentration and the prostatic tissue concentration in the six cases of CTX-injected patients were also determined by high performance liquid chromatography (HPLC). The penetration rate into the prostatic tissue was obtained by the formula; the penetration rate = the prostatic tissue concentration/the serum concentration. The prostatic tissue concentrations determined by the bioassay method were, 36.9 +/- 10.6 micrograms/g at 30 minutes after the injection of 2 g of LMOX and 28.0 +/- 9.0 micrograms/g at 60 minutes, 31.0 +/- 8.3 micrograms/g at 30 minutes after the injection of 1 g of CPZ and 21.1 +/- 10.0 micrograms/g at 60 minutes, and 8.8 +/- 4.1 micrograms/g at 30 minutes after the injection of 2 g of CTX and 4.5 +/- 2.0 micrograms/g at 60 minutes (mean +/- S.D.). The penetration rates determined by the bioassay method were 36.2 +/- 10.9% at 30 minutes after the injection of LMOX and 34.8 +/- 15.3% at 60 minutes, 43.6 +/- 14.4% at 30 minutes after the injection of CPZ and 39.7 +/- 24.1% at 60 minutes, and 11.1 +/- 4.1% at 30 minutes after the injection of CTX and 9.6 +/- 3.8% at 60 minutes (mean +/- S.D.). The penetration rate of CPZ and LMOX were significantly higher than that of CTX (P less than 0.05, P less than 0.01). In 6 of the 14 CTX-injected patients, the serum and prostatic tissue concentrations of CTX and its metabolite, desacetyl-CTX, were also determined by HPLC. The penetration rate of CTX into the prostatic tissue was obtained by the formula; the penetration rate of CTX = the prostatic tissue concentration (CTX + Desacetyl-CTX)/the serum concentration (CTX + Desacetyl-CTX).(ABSTRACT TRUNCATED AT 400 WORDS) 
650 4 |a English Abstract 
650 4 |a Journal Article 
650 7 |a Cefoperazone  |2 NLM 
650 7 |a 7U75I1278D  |2 NLM 
650 7 |a Cefotaxime  |2 NLM 
650 7 |a N2GI8B1GK7  |2 NLM 
650 7 |a Moxalactam  |2 NLM 
650 7 |a VUF6C936Z3  |2 NLM 
700 1 |a Kinukawa, T  |e verfasserin  |4 aut 
700 1 |a Matsuura, O  |e verfasserin  |4 aut 
700 1 |a Hattori, R  |e verfasserin  |4 aut 
700 1 |a Hasegawa, S  |e verfasserin  |4 aut 
700 1 |a Ohshima, S  |e verfasserin  |4 aut 
700 1 |a Ono, Y  |e verfasserin  |4 aut 
773 0 8 |i Enthalten in  |t Hinyokika kiyo. Acta urologica Japonica  |d 1962  |g 32(1986), 12 vom: 30. Dez., Seite 1831-41  |w (DE-627)NLM012631779  |x 0018-1994  |7 nnas 
773 1 8 |g volume:32  |g year:1986  |g number:12  |g day:30  |g month:12  |g pages:1831-41 
912 |a GBV_USEFLAG_A 
912 |a SYSFLAG_A 
912 |a GBV_NLM 
912 |a GBV_ILN_20 
912 |a GBV_ILN_22 
912 |a GBV_ILN_40 
912 |a GBV_ILN_60 
912 |a GBV_ILN_72 
912 |a GBV_ILN_120 
912 |a GBV_ILN_350 
912 |a GBV_ILN_2001 
912 |a GBV_ILN_2003 
912 |a GBV_ILN_2005 
912 |a GBV_ILN_2006 
912 |a GBV_ILN_2008 
912 |a GBV_ILN_2010 
912 |a GBV_ILN_2012 
912 |a GBV_ILN_2018 
951 |a AR 
952 |d 32  |j 1986  |e 12  |b 30  |c 12  |h 1831-41