与氧化并发的简单悬浮剂中的β-乳糖抗生素的化学稳定性研究
Ginjiro Kato1, Hidemichi Mitome1, Syu Takeda1
1Laboratory of Pharmaceutical Analytical Chemistry, College of Pharmaceutical Sciences, Matsuyama University, 4-2 Bunkyo-cho, Matsuyama, Ehime, 790-8578, Japan.
Journal of pharmaceutical health care and sciences
|November 19, 2024
概括
与氧化同时悬浮阿莫西西林会降解抗生素,尤其是在长时间浸泡时. 在性条件下,Cefcapene pivoxil的溶解度也会降低,影响药物输送.
科学领域:
- 制药科学 制药科学
- 药物的稳定性 药物的稳定性
- 老年医学 老年医学
背景情况:
- 简单的悬浮方法是常见的老年患者的消化不良.
- 有限的数据存在于同悬浮剂的药物稳定性,特别是与酸性或性配方.
- 长时间浸泡可能会影响药物的稳定性.
研究的目的:
- 为了研究与氧化 (MgO) 联合悬浮中的阿莫西西林和Cefcapene pivoxil 化的化学稳定性.
- 评估长时间浸泡对这些同悬浮剂药物稳定性的影响.
主要方法:
- 氨基西林和 cefcapene pivoxil 化物被悬浮在温水中,有或没有MgO.
- 样品被浸泡了10分钟或5小时.
- 使用高性能液态色谱 (HPLC) 进行分析,并通过质谱和NMR识别了降解产物.
主要成果:
- 当与MGO联合悬浮时,氨基西林部分降解为氨基西林酸和氨基西林二基托皮佩拉зин.
- 随着浸泡时间的延长,阿莫西西林的降解会增加.
- 由于MgO共同悬浮中的溶解性差,Cefcapene pivoxil的回收率下降;没有观察到降解.
结论:
- 由于阿莫西西林的化学不稳定性,阿莫西西林和MgO应分别暂停使用.
- 长时间浸泡会导致阿莫西西林的降解风险.
- 在性条件下,烯氧的溶解性较差可能会影响吸收和管道服药.
更多相关视频
相关概念视频
Factors Affecting Dissolution: Polymorphism, Amorphism and Pseudopolymorphism
287
Polymorphism refers to the existence of a drug substance in multiple crystalline forms, known as polymorphs. Recently, this term has been expanded to include solvates (forms containing a solvent), amorphous forms (non-crystalline forms), and desolvated solvates (forms from which the solvent has been removed).
Some polymorphic crystals possess lower aqueous solubility than their amorphous counterparts, leading to incomplete absorption. For instance, the oral suspension of Chloramphenicol, which...
Some polymorphic crystals possess lower aqueous solubility than their amorphous counterparts, leading to incomplete absorption. For instance, the oral suspension of Chloramphenicol, which...
287
Complexation Equilibria: Factors Influencing Stability of Complexes
343
In complexation reactions, metal cations are the electron pair acceptors, and the ligands are the electron pair donors. The stability of the metal complexes depends primarily on the complexing ability of the central metal ion and the nature of the ligands. Generally, the complexing ability of the metal ion depends on the size and charge of the ion. As the metal ion size increases, the stability of the metal complexes decreases, provided that the valency of the metal ion and the ligands remain...
343
Factors Affecting Dissolution: Drug Permeability, Stability and Stereochemistry
178
Orally administered drugs primarily enter the systemic circulation via passive diffusion through the intestinal membranes. The drug's absorption is influenced by drug stability in the gastrointestinal GI tract, membrane permeability, the surface area available for absorption, luminal drug concentration, and residence time in the lumen. Drug permeability can be enhanced by adjusting the lipophilicity, polarity, or molecular size of the drug, promoting its passive transport across intestinal...
178
Common Ion Effect
41.1K
Compared with pure water, the solubility of an ionic compound is less in aqueous solutions containing a common ion (one also produced by dissolution of the ionic compound). This is an example of a phenomenon known as the common ion effect, which is a consequence of the law of mass action that may be explained using Le Châtelier’s principle. Consider the dissolution of silver iodide:
41.1K
EDTA: Auxiliary Complexing Reagents
555
EDTA titrations are usually carried out in highly basic conditions, where the fully deprotonated form of EDTA, Y4−, actively complexes with the free metal ions in the solution. Several metal ions precipitate as hydrous oxide (hydroxides, oxides, or oxyhydroxides) under these conditions, lowering the concentration of free metal ions in the solution. For this reason, auxiliary complexing agents or ligands such as ammonia, tartrate, citrate, or triethanolamine are used in EDTA titrations to...
555
Ionic Strength: Effects on Chemical Equilibria
1.4K
The addition of an inert ionic compound increases the solubility of a sparingly soluble salt. For example, adding potassium nitrate to a saturated solution of calcium sulfate significantly enhances the solubility of calcium sulfate. Le Châtelier's principle cannot predict this shift in the equilibrium. Instead, this could be explained in terms of changes in the effective concentration of the ions in solution in the presence of added inert salt.
In this solution, the primary...
In this solution, the primary...
1.4K


