中华实验眼科杂志
中華實驗眼科雜誌
중화실험안과잡지
CHINESE JOURNAL OF EXPERIMENTAL OPHTHALMOLOGY
2011年
8期
676-680
,共5页
瞿玲辉%李良毛%谢汉平%潘峰
瞿玲輝%李良毛%謝漢平%潘峰
구령휘%리량모%사한평%반봉
两性霉素B%色谱法%高效液相%药代动力学
兩性黴素B%色譜法%高效液相%藥代動力學
량성매소B%색보법%고효액상%약대동역학
Amphotericin B%Chromatography%High pressure liquid%Pharmacokinetics
背景 角膜基质内注射或前房内注射两性霉素B治疗顽固的真菌性角膜炎取得较好疗效,但通过这2种途径给药后,药物在角膜和房水的浓度变化尚不清楚.目的 探讨质量分数0.25%两性霉素B滴眼液点眼、1%两性霉素B注射液角膜基质内注射及1%两性霉素B注射液前房内注射3种途径给药后兔眼角膜和房水中的药物质量浓度变化.方法 健康家兔45只按随机数字表法分为A、B、C 3组,每组15只.A组、B组分别在角膜基质内和前房内单次注射10 μg两性霉素B注射液,C组兔眼机械法去除角膜上皮后用0.25%两性霉素B滴眼液点眼,每次50μl,共6次,每次间隔5 min.分别于用药后30 min、6 h、1 d、3 d、7 d各处死3只实验兔,获取房水和角膜组织,采用高效液相色谱法进行两性霉素B质量浓度的定量检测.结果 在质量浓度0.10~100.00 mg/L范围内,两性霉素B的峰面积与吸收度之间具有良好的线性关系;0.10mg/L为其定量限质量浓度;药物在房水的回收率为89.1%~95.7%,在角膜中为81.4%~83.6%.用药后30 min、6 h、1 d A组角膜中的药物质量分数高于B组及C组,差异均有统计学意义(P<0.05),高药物质量浓度可持续7 d,超出绝大多数敏感真菌的MIC90.用药后30 min、6 h、1 d B组兔眼房水中的药物质量浓度高于A组及C组,差异均有统计学意义(P<0.05).C组1 d内角膜和房水中均检测到明显药物浓度.结论 兔眼角膜基质内注射及前房内注射两性霉素B可以提高药物在角膜及房水中的质量浓度,清除角膜上皮可以提高两性霉素B的角膜穿透力.
揹景 角膜基質內註射或前房內註射兩性黴素B治療頑固的真菌性角膜炎取得較好療效,但通過這2種途徑給藥後,藥物在角膜和房水的濃度變化尚不清楚.目的 探討質量分數0.25%兩性黴素B滴眼液點眼、1%兩性黴素B註射液角膜基質內註射及1%兩性黴素B註射液前房內註射3種途徑給藥後兔眼角膜和房水中的藥物質量濃度變化.方法 健康傢兔45隻按隨機數字錶法分為A、B、C 3組,每組15隻.A組、B組分彆在角膜基質內和前房內單次註射10 μg兩性黴素B註射液,C組兔眼機械法去除角膜上皮後用0.25%兩性黴素B滴眼液點眼,每次50μl,共6次,每次間隔5 min.分彆于用藥後30 min、6 h、1 d、3 d、7 d各處死3隻實驗兔,穫取房水和角膜組織,採用高效液相色譜法進行兩性黴素B質量濃度的定量檢測.結果 在質量濃度0.10~100.00 mg/L範圍內,兩性黴素B的峰麵積與吸收度之間具有良好的線性關繫;0.10mg/L為其定量限質量濃度;藥物在房水的迴收率為89.1%~95.7%,在角膜中為81.4%~83.6%.用藥後30 min、6 h、1 d A組角膜中的藥物質量分數高于B組及C組,差異均有統計學意義(P<0.05),高藥物質量濃度可持續7 d,超齣絕大多數敏感真菌的MIC90.用藥後30 min、6 h、1 d B組兔眼房水中的藥物質量濃度高于A組及C組,差異均有統計學意義(P<0.05).C組1 d內角膜和房水中均檢測到明顯藥物濃度.結論 兔眼角膜基質內註射及前房內註射兩性黴素B可以提高藥物在角膜及房水中的質量濃度,清除角膜上皮可以提高兩性黴素B的角膜穿透力.
배경 각막기질내주사혹전방내주사량성매소B치료완고적진균성각막염취득교호료효,단통과저2충도경급약후,약물재각막화방수적농도변화상불청초.목적 탐토질량분수0.25%량성매소B적안액점안、1%량성매소B주사액각막기질내주사급1%량성매소B주사액전방내주사3충도경급약후토안각막화방수중적약물질량농도변화.방법 건강가토45지안수궤수자표법분위A、B、C 3조,매조15지.A조、B조분별재각막기질내화전방내단차주사10 μg량성매소B주사액,C조토안궤계법거제각막상피후용0.25%량성매소B적안액점안,매차50μl,공6차,매차간격5 min.분별우용약후30 min、6 h、1 d、3 d、7 d각처사3지실험토,획취방수화각막조직,채용고효액상색보법진행량성매소B질량농도적정량검측.결과 재질량농도0.10~100.00 mg/L범위내,량성매소B적봉면적여흡수도지간구유량호적선성관계;0.10mg/L위기정량한질량농도;약물재방수적회수솔위89.1%~95.7%,재각막중위81.4%~83.6%.용약후30 min、6 h、1 d A조각막중적약물질량분수고우B조급C조,차이균유통계학의의(P<0.05),고약물질량농도가지속7 d,초출절대다수민감진균적MIC90.용약후30 min、6 h、1 d B조토안방수중적약물질량농도고우A조급C조,차이균유통계학의의(P<0.05).C조1 d내각막화방수중균검측도명현약물농도.결론 토안각막기질내주사급전방내주사량성매소B가이제고약물재각막급방수중적질량농도,청제각막상피가이제고량성매소B적각막천투력.
Background Intracameral or intracorneal administration of amphotericin B (AMB) can achieve significant therapeutic efficacy in the treatment of recalcitrant fungal keratitis in cases that do not respond to conventional antifungal therapy. However, the ocular pharmacokinetics of the two routes of administration is unclear.Objective The goal of this study was to investigate the level of amphotericin B in cornea and aqueous humor of rabbits after administration of AMB via three different routes. Methods Forty-five healthy domestic rabbits were randomly divided into three groups. 1% amphotericin B of 10 μg was intrastromally or intracamerally injected into 15 rabbits, respectively,in group A and group B. Topical 0. 25% amphotericin B was topically administered to the eyes with corneal epithelial debridement (group C). Experimental animals were sacrificed and the corneas and aqueous humor samples were obtained for the detection of levels of amphotericin B at 30 minutes,6 hours, 1 day,3 and 7 days by high-performance liquid chromatography (HPLC). Results Calibration curves were linear over the range of 0. 10-100. 00 mg/L. The concentration of 0. 10 mg/L was the lowest quantifiable limit. The recovery of amphotericin B ranged from 89. 1% -95.7% from aqueous humor samples and 81.4% -83.6% from the cornea samples. After a single injection,effective drug levels were achieved and maintained for 7 days in cornea in group A, exceeding the minimum inhibitory concentration at which 90% of isolates are inhibited (MIC90) for a wide spectrum of fungi and molds with significant differences in comparison with group B and group C ( P<0. 05 ). Effective drug levels were achieved in the aqueous humor in group B at 30 minutes after a single injection, but drug levels decreased dramatically within 6 hours. The evident differences were found between group B and group A or group C (P< 0.05). A considerable amount of amphotericin B was detected in the cornea and aqueous humor in group C within 1 day.Conclusion Effective high drug levels can be reached in rabbit cornea and aqueous humor after intrastromal and intracameral injection, respectively. Penetration of topical amphotericin B was greatly elevated after epithelial debridement.