卡内多霉素是一种很稳定的抗生素，其粉沫置于密封容器中，在室温下保存二年以上，活性不减。
Kanendomycin is a very stable antibiotic, and its activity does not decrease when the powder is placed in an airlight container and kept at room temperatures for more than 2 years.
目的研究1,6二磷酸果糖(FDP)对阿霉素(adm)导致大鼠心肌酪氨酸硝基化的影响。
AIM to study the effect of fructose 1, 6 diphosphate (FDP) on adriamycin (ADM) induced myocardial tyrosine nitration in rats.
目的研究1,6二磷酸果糖(FDP)对阿霉素(adm)导致大鼠心肌细胞凋亡的影响。
AIM to study the effect of fructose 1, 6 diphosphate (FDP) on adriamycin (ADM) induced cardiomyocyte apoptosis in rats.
目的用迭代二步法估算肌注妥布霉素的群体药动学参数。
OBJECTIVE to estimate the population pharmacokinetic parameters of tobramycin by iterative two stage method.
青霉素发酵过程是一个具有二次微生物代谢的生化过程，机理复杂，影响因素繁多。
The penicillin fermentation process is a very complicated biochemical process accompanied with secondary microbial metabolism, which is affected by many factors.
目的：研究人参二醇组皂苷(PDS)减轻庆大霉素(gm)性肾损伤的机制。
OBJECTIVE: To study the mechanism of Panaxadiol saponins (PDS) in treating renal injury induced by Gentamicin (GM).
制药生产工艺的放大是化学工程一个重要的成功的范例，例如在二次世界大战中，青霉素的大批量供应拯救了很多人。
Sealing up PC production processes is major success story for chemical engineering. For example the bulk supply of penicillin in World War II has helped many.
结果：骨碎补液可使链霉素所致耳蜗一回和二回毛细胞的损伤减轻。
Result Gusuibu decreased the loss of outer hair cells in the first and second coils.
目的采用反相高效液相色谱（RP-HPLC）法测定氯霉素滴眼液中氯霉素的含量及有关物质中二醇物和对硝基苯甲醛的含量。
Objective To develop a quantitative method for the determination of chlorampenicol and related substances, such as glycols and p-nitrobenzaldehyde, in chlorampenicol eye drops by RP-HPLC.
第二天，这位苏格兰细菌学家发现玻璃器皿里有一块地方很干净。在那块地方霉菌里的青霉素将细菌杀死了。 ！
The following day, theScottish bacteriologist found in the dish a clear area where thepenicillin in the mold had been killing bacteria.
本研究评价了米卡芬净、两性霉素B和伏立康唑单独用药，二联用药和三联用药治疗播散性多育赛多孢感染鼠类模型的疗效。
We have evaluated the efficacies of micafungin, amphotericin B, and voriconazole, alone and in double and triple combinations, in a murine model of systemic infection by Scedosporium prolificans.
研究阿齐霉素磷酸二氢钠对临床常见致病菌的体外抗菌作用效果，并与阿齐霉素抗菌效果进行比较。
To study the anti-bacteria effects of Azithromycin sodium dihydrogen phosphate on common clinical pathogens in vitro and compare it with Azithromycin.
应用试管二倍稀释法测定了氟砜霉素、氯霉素、TMP和OMP对15株畜禽常见病原菌的最小抑菌浓度（ MIC）。
The MIC determinations of florfenicol, chloramphenicol, TMP and OMP, against1 5iso- lates of veterinary origin were performed using the method of broth two-fold dilutions firstly.
方法以替硝唑、氯霉素为主药，卡波姆-940、丙二醇等为辅料制备凝胶；采用双波长分光光度法测定主药含量。
Methods Tinidazole and chloromycetin were used as the principal agents, carbomer-940, propylene glycol as preservatives to prepare compound tinidazole gel.
采用矩量法确定了盐酸大观霉素溶析结晶二次成核和晶体生长动力学经验方程。
The empirical equations for secondary nucleation and crystal growth kinetics were determined by moment method.
到了二战结束，青霉素已被广泛用于民用和战场中。
By the end of Would War II, penicillin was available in large amounts, for civilian as well as military use.
本发明涉及两种二聚桔霉素类化合物的制备方法和用途。
The invention relates to a preparation method and a use of two dimer citrinin compounds.
生产方法包括将赤霉素用乙醇溶解，然后加入磷酸二氢钾，再加入水，即得产品。
The production process includes dissolving gibberellin in ethanol, adding potassium dihydrogen phosphate, and adding water to obtain the product.
本发明的维斯丽痤疮酊组成有甲硝唑磷酸二钠、水杨酸、氯霉素和75%酒精。
Weisili acne tincture comprises metronidazole disodium hydrogen phosphate, salicylic acid, chloramphenicol and 75 percent alcohol.
本文克隆了赤霉素生物合成途径中关键合成酶：贝壳杉烯氧化酶和20-氧化酶，并研究了二者在果树生长发育中的表达规律。
In this article we cloned two crucial gibberellins biosynthesis enzyme genes: ent - kaurene oxidase and 20 - oxidase, and we investigated their expression patterns. 1.
本试验取硫酸庆大霉素注射液，按《中国药典》2005年版二部附录所载的“无菌检查法”项下进行方法学验证试验。
According to the "sterile test method" which is recorded in the appendix in Chinese Pharmacopoeia (2005 Edition), the methodology validation is experimented with Gentamycin sulfate injection.
用于合成埃坡霉素及其衍生物并经保护的3，5-二羟基-2，2-二甲基-戊酰胺及其制备方法和应用。
Protected 3,5-dihydroxy-2,2-dimethyl-valeroamides for the synthesis of epothilones and derivatives and process for the production and the use.
用于合成埃坡霉素及其衍生物并经保护的3，5-二羟基-2，2-二甲基-戊酰胺及其制备方法和应用。
Protected 3,5-dihydroxy-2,2-dimethyl-valeroamides for the synthesis of epothilones and derivatives and process for the production and the use.
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