首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 546 毫秒
1.
目的:采用HPLC法测定兽用盐酸林可霉素注射液中林可霉素的含量。方法:用XBridge C18色谱柱(250 mm×4.6 mm,5μm),以0.05 moL/L硼砂溶液(用85%磷酸溶液调节pH值至6.0)-甲醇(4∶6)为流动相,检测波长214 nm。结论:在0.4738~3.7900 mg/mL的浓度范围内,林可霉素线性关系良好,回归方程Y=159000X+52600,r2=0.9997,精密度试验RSD为0.20%(n=6),重复性试验RSD为0.36%(n=6)。结论:本方法简便,灵敏,能有效缩短兽用盐酸林可霉素注射液中林可霉素含量的检测时间,提高工作效率。  相似文献   

2.
建立并验证HPLC法测定盐酸林可霉素注射液的含量方法。采用十八烷基硅烷键合硅胶色谱柱(4.6 mm×250 mm,5μm),以磷酸溶液-乙腈-甲醇(80∶15∶15)为流动相,流速为1.0 mL/min,柱温为40℃,波长210 nm。试验结果表明,盐酸林可霉素在0.1~4.0 mg/mL范围内线性良好,R=0.999 9,平均回收率为98.8%(n=9),RSD为1.0%。该方法与《中华人民共和国兽药典》2015年版一部中的HPLC法比较,可减少盐溶液对色谱柱的污染,提高色谱系统的稳定性、灵敏度及被测色谱峰的理论塔板数,同时流动相配置方便、快速,适用于盐酸林可霉素注射液的质量控制。  相似文献   

3.
建立了兽用林可霉素注射液中非法添加盐酸左旋咪唑的高效液相色谱检测方法。采用Waters Atlantis? T3 C18(4.6×250mm, 5μm)色谱柱分离,以磷酸二氢钠溶液-甲醇(70:30)作为流动相进行等度洗脱(流速1.00mL/min),用二极管阵列检测器在230nm波长处进行测定。考察了此色谱条件下方法的专属性、线性、回收率、精密度、检测限和耐用性。结果表明,盐酸左旋咪唑在进样浓度为0.02mg/mL~0.4mg/mL时呈良好的线性关系,R2=0.9999;重复性试验RSD为0.6%;平均回收率为99.7%;检测限为 0.0002mg/mL,定量限为0.0016mg/mL。该法准确、简便、可行,适用于林可霉素注射液中盐酸左旋咪唑的检测。  相似文献   

4.
本试验建立了鱼腥草、柴胡、维生素C、盐酸林可霉素、黄芪多糖等注射液中非法添加地塞米松磷酸钠的超高效液相色谱检查方法。采用Waters ACQUITY UPLC® BEH C18色谱柱(2.1 mm×50 mm,1.7 μm),以0.75%三乙胺溶液(磷酸调节pH 3.0)-甲醇-乙腈(50:45:5)为流动相,流速0.3 mL/min,二极管阵列检测器,波长采集范围为190~400 nm,记录色谱图波长242 nm,柱温25℃,进样量10 μL。地塞米松磷酸钠质量浓度在10.0~200.0 mg/L内峰面积呈良好线性关系(R2=0.9999),在鱼腥草、柴胡、维生素C、盐酸林可霉素、黄芪多糖等注射液中地塞米松磷酸钠的平均回收率和相对标准偏差(RSD)分别为97.54%和1.14%、101.59%和0.19%、100.92%和0.92%、99.82%和0.73%、100.08%和0.62%。本方法简单、快速、灵敏、可靠,适用于鱼腥草等5种注射液中非法添加地塞米松磷钠的检查。  相似文献   

5.
建立了测定氟苯尼考注射液中氟苯尼考含量的高效液相色谱法。采用C18色谱柱(4.6 mm×150 mm,5μm),流动相为甲醇∶水(pH值为3.0)为40∶60(v/v),流速为1 mL/min,检测波长为222 nm,进样10μL,柱温为室温。氟苯尼考浓度在0.1-3 mg/mL范围内,峰面积与浓度的线性关系良好(R^2=0.999 6);平均回收率为99.49%,RSD为1.12%(n=4)。此法简便、快速、灵敏度高、重现性好。  相似文献   

6.
建立了测定林可霉素-大观霉素复方油混悬注射液中盐酸林可霉素与盐酸大观霉素含量的高效液相色谱(HPLC)方法.采用C18色谱柱(4.6mm×250 mm,5 μm),检测林可霉素的流动相为0.05mol/L硼砂溶液(用850 mL/L磷酸调节pH至5.0)-甲醇-乙腈(60∶36∶4),检测波长为214 nm;检测大现霉...  相似文献   

7.
高效液相色谱法测定盐酸林可霉素注射液的含量   总被引:1,自引:0,他引:1  
建立盐酸林可霉素注射液含量测定的高效液相色谱法。色谱柱:C_(18)色谱柱(4.6 mm×250 mm,5μm),流动相:0.05 mol/L硼砂溶液(用85%磷酸溶液调节pH值至5.0)∶甲醇∶乙腈=67∶33∶2(V/V),流速:1 mL/min,检测波长:214 nm,进样量:10μL,柱温:30℃。盐酸林可霉素浓度在0.1-2 mg/m L范围内峰面积与浓度的线性关系良好(R~2=0.999 9)。此法简便、快捷、灵敏度高、重现性好。  相似文献   

8.
建立盐酸左旋咪唑片中盐酸左旋咪唑含量测定的高效液相色谱法。采用Agilent Eclipse XDB-C18(250 mm×4.6 mm),5μm色谱柱,Agilent 1260DAD检测器,流动相为0.05 mol/L磷酸二氢钾溶液(三乙胺调节pH值至7.0)-乙腈(80∶20,v/v);进样量为20μL;柱温为30℃;流速为1.0 mL/min;检测波长为214nm。结果表明:盐酸左旋咪唑在1.024~102.398μg/mL范围内线性关系良好(r=1.0000),高、中、低浓度回收率分别为97.4%、99.7%、99.3%。该方法定性、定量准确,适用于盐酸左旋咪唑片中盐酸左旋咪唑的含量测定。  相似文献   

9.
建立了苦参注射液中苦参碱含量的HPLC检测法。色谱柱为waters C18(4.6 mm×150 mm,5μm),0.02 mol/L乙酸铵缓冲溶液(含500μL/L三乙胺)-甲醇-乙腈(70∶10∶20)为流动相,检测波长210 nm,流速1 mL/min,柱温30℃,进样量20μL。苦参碱进样浓度在4.0~200.0μg/mL范围内与峰面积呈良好的线性关系(r=0.999 9);样品平均回收率为100.1%(n=9),RSD为1.1%。本方法简便、准确度高、重复性好,可用于苦参注射液中苦参碱的质量控制。  相似文献   

10.
为了建立柴胡注射液、维生素C注射液、盐酸林可霉素注射液、黄芪多糖注射液中非法添加倍他米松的超高效液相色谱检查方法,采用Waters ACQUITY UPLCBEH C18色谱柱(2.1 mm×50 mm,1.7μm),以0.75%三乙胺溶液(用磷酸调节p H为3.0)-甲醇-乙腈(50∶45∶5)为流动相;流速为0.3 m L·min-1;二极管阵列检测器,波长采集范围为190~400 nm,记录色谱图波长242 nm。柱温25℃,进样量10μL。倍他米松质量浓度在20.0~180.0 mg·L-1内峰面积呈良好线性关系(R2=0.9997,n=7),在柴胡注射液、盐酸林可霉素注射液、维生素C注射液、黄芪多糖注射液中倍他米松的平均回收率分别为103.5%(RSD=0.2%)、101.2%(RSD=0.8%)、100.4%(RSD=1.7%)、99.2%(RSD=1.7%)。本方法简便、快速、准确,可用于柴胡注射液等四种兽用注射液中非法添加倍他米松的检测。  相似文献   

11.
Mammary excretion of lincomycin in cows   总被引:1,自引:0,他引:1  
  相似文献   

12.
13.
Treatment of virulent footrot with lincomycin and spectinomycin   总被引:1,自引:0,他引:1  
A mixture of lincomycin and spectinomycin was investigated as a treatment for footrot in sheep. In a controlled clinical trial 92.5% of acute and chronic cases of virulent footrot were cured following a single intramuscular injection of a mixture containing 50 mg lincomycin and 100 mg spectinomycin/ml at a dose rate of 1 ml/10 kg bodyweight. No improvement in clinical response was observed in groups of sheep treated on 3 successive days with this dose rate nor in another group treated once at a dose rate 1 ml/3.3 kg bodyweight. Cure effectiveness of each of the 3 treatment groups relative to untreated controls was 89%, 95% and 95%. Efficacy of lincomycin/spectinomycin was compared with that of penicillin/streptomycin in the treatment of footrot on 2 farms in south western New South Wales. Assessments made 14 to 17 d after treatment showed that on one farm all 122 ewes treated with lincomycin/spectinomycin had recovered while 170 of 175 ewes treated with penicillin/streptomycin recovered in the same period. On the second farm 87 of 90 ewes treated with lincomycin/spectinomycin recovered, compared with 184 of 190 sheep in the same flock treated with penicillin/streptomycin. Supportive footbathing did not seem to improve the clinical response in either treatment group and the paring done was sufficient only to establish diagnosis and to remove grossly overgrown horn.  相似文献   

14.
15.
16.
分析了涉嫌非法添加的盐酸林可霉素注射液检测中存在的问题并提出了建议。盐酸林可霉素注射液中的非法添加物,不仅增加了动物产品药物残留的风险,还导致含量测定时色谱峰出现不同变化,使每次检测结果出现巨大差异。严厉打击此种行为需从制度和技术上加以完善。  相似文献   

17.
18.
1. The effects of adding lincomycin to either the food (2.2 mg/kg) or drinking water (equivalent or 0.5 equivalent amount) of male broiler chicks were examined. 2. There were four treatments: control (no lincomycin), diet containing 2.2 mg lincomycin/kg, control diet plus drinking water containing lincomycin at concentrations calculated to provide an intake equivalent to treatment 2, and treatment 14 with lincomycin concentration reduced by half. 3. There was no significant effect of any treatment upon mortality, efficiency of food utilisation at 42 d of age, final body weights or monetary indices. 4. Analyses of breast, thigh and liver tissues, using a method with a sensitivity of 1.0 mg/kg, failed to reveal any evidence of lincomycin residues. 5. It is concluded that the use of lincomycin at 2.2 mg/kg may not be effective in improving either the biological or economic performance of the broiler chicken.  相似文献   

19.
研究制定高效液相色谱法测定饲料添加剂中盐酸林可霉素含量的方法。采用waters2695高效液相色谱仪,C18色谱柱(150 mm×4.6 mm,5μm);以0.05 mol/l硼砂溶液:甲醇(55:45)为流动相;流速:1.0 ml/min;检测波长:214 nm。主峰和相邻峰有较好的分离;盐酸林可霉素在14.7~492μg/ml范围内线形良好,R2=0.998 7(n=6),检测限为0.15μg,平均回收率分别为98.7%、99.5%、99.1%。该方法快速、灵敏、可靠,可用于饲料添加剂中盐酸林可霉素的含量测定。  相似文献   

20.
Lincomycin 10 mg kg?1, IV in buffalo calves followed two-compartment open model with high distribution rate constant α (11.2?±?0.42 h?1) and K 12/K 21 ratio (4.40?±?0.10). Distribution half-life was 0.06?±?0.01 h and AUC was 41.6?±?1.73 μg mL?1 h. Large Vdarea (1.15?±?0.03 L kg?1) indicated good distribution of lincomycin in various body fluids and tissues. Peak plasma level of lincomycin (71.8?±?1.83 μg mL?1) was observed at 1 min as expected by IV route. The elimination half-life and MRT of lincomycin were short (3.30?±?0.08 and 4.32?±?0.11 h, respectively). Lincomycin 10 mg kg?1 IV at 12-h interval would be sufficient to maintain T?>?MIC above 60 % for bacteria with minimum inhibitory concentrations (MIC) values ≤1.6 μg mL?1. Favourable pharmacokinetic profile in buffalo calves and a convenient dosing interval suggest that lincomycin may be an appropriate antibacterial in buffalo species for gram-positive and anaerobic bacterial pathogens susceptible to lincomycin.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号