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colistimethate sodium (Colistineb / Colobreathe / Colomycin injection)

✓ Approved

Forest Laboratories Inc. · 治疗药物

什么是 colistimethate sodium?

colistimethate sodium 是一种治疗药物,由Forest Laboratories Inc.研发。该药已获批,用于治疗相关适应症,给药途径:Inhaled、Injectable (Others)、Intravenous (IV)。

药物档案

商品名Colistineb, Colobreathe, Colomycin injection
公司Forest Laboratories Inc.
给药途径Inhaled, Injectable (Others), Intravenous (IV)
状态Approved

治疗适应症

colistimethate sodium 针对 1 个适应症,涉及 1 个治疗领域。

治疗领域疾病/病症分期
Infections and infestationsPneumonia pseudomonal✓ Approved

相关研究文献

PubMedApplied and environmental microbiology2026-08-05

Sodium ion stress accelerates cell lysis in Bacillus coagulans by exacerbating energy deficit during carbon source transition.

Liu Zhihao Z, Zhuang Yingping Y, Wang Yonghong Y, Wang Guan G

The choice of pH neutralizer plays a critical role in determining the performance of industrial lactic acid fermentation. This study investigated the distinct phenotypic and metabolic responses of Bacillus coagulans during batch fermentation with mixed carbon sources (glucose and trehalose) when using sodium hydroxide versus calcium hydroxide for pH control. Compared to calcium hydroxide, sodium hydroxide resulted in a slightly lower lactic acid yield and induced significant cell lysis during the carbon source transition. Metal ion experiments confirmed that sodium ion stress is the primary factor responsible for extensive cell lysis. Omics analysis indicated that under sodium hydroxide conditions, cells require more energy to resist stress. To meet this demand, cells downregulated cellular growth and sodium ion uptake systems, while upregulating carbon source transport. However, during carbon source transition, cellular resource reallocation resulted in insufficient carbon source uptake, leading to stagnation of glycolysis and amino acid metabolism. The resulting energy deficit triggered upregulation of cellular hydrolases, ultimately causing population-wide cell lysis. In contrast, calcium hydroxide as a neutralizer does not impose sodium stress and contributes to maintaining cell wall stability under carbon source deficiency. This study contributes to the understanding of cellular regulatory mechanisms in response to different neutralizers, and provides insights for metabolic engineering and process optimization.IMPORTANCEpH neutralizer selection critically determines cell survival and process efficiency in industrial fermentation. Our study demonstrates that sodium hydroxide, although effective for pH control, imposes severe sodium ion stress that synergizes with the inherent energy vulnerability of cells during carbon source transition, triggering catastrophic population-wide lysis in Bacillus coagulans. Through integrated physiology, ion experiments, and multi-omics analyses, we reveal that the underlying cause is an energy crisis arising from the conflict between stress defense and metabolic reallocation. In contrast, calcium hydroxide not only avoids sodium stress but also confers structural and thermal stability to cells, thereby preserving cell density and improving carbon utilization. These findings shift the perspective on neutralizers from mere pH regulators to key determinants of cellular energy economy and survival. Our study thus offers a rational basis for neutralizer selection, strain engineering toward ion resistance, and the design of robust fermentation processes, with direct implications for the sustainable and cost-effective production of lactic acid and other microbial metabolites.

PMID 42554496
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PubMedJournal of the science of food and agriculture2026-08-05

Study on the changes and mechanisms on the quality of beef tripe during tenderization.

Yu Peipei P, Zhu Shijin S, Wang Lishi L, Gao Pei P et al.

The quality characteristics of salted beef tripe were investigated throughout the multi-stage tenderization process, encompassing cleaning, pre-cooking, alkaline treatment (sodium carbonate), water soaking and final cooking. The underlying tenderization mechanism was elucidated through the assessment of collagen content, water status and microstructural evolution. Alkaline treatment with sodium carbonate functions as a highly effective approach to tenderize salted beef tripe. Morphological observations demonstrated a sequential transformation characterized by tissue expansion post-washing, followed by contraction after pre-cooking. Sodium carbonate treatment served as the pivotal tenderization step, inducing pronounced tissue swelling and structural integrity. Water distribution analysis revealed significant dynamic shifts in free and immobile water proportions during tenderization. Free water exhibited an initial increase, followed by a decrease and subsequent rebound, whereas immobile water inversely decreased, increased and then declined. Scanning electron microscopy revealed structural evolution in salted beef tripe: transitioning from a compact morphology to distinct muscle fiber organization post-cleaning, followed by fiber fragmentation after sodium carbonate treatment. Texture analysis demonstrated a substantial reduction in shear force confirming the efficacy of alkaline tenderization. This study provided a theoretical and practical basis for controlling the tenderization process and quality of salted beef tripe. © 2026 Society of Chemical Industry.

PMID 42554220
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PubMedCureus2026-08-05

Acute Phosphate Nephropathy Following Oral Sodium Phosphate Bowel Preparation.

Oztop Enes E

Acute phosphate nephropathy (APN) is a rare but important cause of acute kidney injury (AKI), most commonly associated with the use of oral sodium phosphate bowel preparations administered prior to colonoscopy. In this report, we describe the case of a 60-year-old female patient who developed severe AKI necessitating temporary hemodialysis after bowel preparation with a phosphate-containing laxative. Quick identification, cessation of nephrotoxic agents, aggressive intravenous hydration, and supportive hemodialysis therapy facilitated gradual renal recovery. This case points out the importance of heightened awareness of APN, particularly in patients with multiple predisposing factors.

PMID 42553916
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PubMedCureus2026-08-05

Hyponatremia as a Prognostic Marker in Cirrhosis: A Systematic Review of Its Role Beyond the Model for End-Stage Liver Disease in Predicting Mortality.

Kotte Mounika M, Nashed Sally M SM, Raj Aryan A, Bansal Vimi V et al.

This systematic review evaluates the prognostic significance of hyponatremia in patients with cirrhosis across diverse clinical settings. A comprehensive literature search was conducted across PubMed/MEDLINE, Scopus, and Web of Science for studies published between January 2000 and December 2025, in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines and a structured Population, Intervention, Comparison, and Outcomes (PICO) framework. Observational cohort studies assessing the association between serum sodium levels and mortality outcomes in adult patients with cirrhosis were included. Seven studies met the eligibility criteria, encompassing heterogeneous cohorts, including critically ill patients, transplant waitlist populations, and individuals with advanced disease states such as refractory ascites. Across the included studies, hyponatremia consistently emerged as an independent predictor of mortality, with prognostic significance observed across varying degrees of disease severity and clinical contexts. Notably, serum sodium demonstrated additional risk-stratification value beyond the Model for End-Stage Liver Disease (MELD) score, particularly among patients with lower MELD scores, suggesting its utility in identifying high-risk individuals who may otherwise be underestimated by conventional prognostic models. From a pathophysiological perspective, hyponatremia reflects underlying circulatory and neurohumoral dysfunction, integrating key features of decompensated liver disease into a single clinically measurable parameter. Despite heterogeneity in study design and definitions of hyponatremia, the included studies generally demonstrated moderate methodological quality. Collectively, these findings support the incorporation of serum sodium into prognostic assessment frameworks while emphasizing the need for cautious interpretation and further research focusing on dynamic sodium trends and multidimensional risk-prediction models.

PMID 42553811
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PubMedThe journal of physical chemistry. C, Nanomaterials and interfaces2026-08-05

Adsorption and Reactivity of Na+ Salt and Room-Temperature Ionic Liquid at Na Metal Surface.

Sarkar Ranjini R, Fasulo Francesca F, Muñoz-García Ana Belén AB, Tirri Bernardino B et al.

Sodium-ion batteries are cost-effective and sustainable alternatives to lithium-ion batteries. Recently, metal anode batteries have gained prominence over metal-ion systems due to their higher theoretical capacities. However, sodium metal batteries employing conventional organic electrolytes face persistent challenges, including dendrite formation and unstable solid-electrolyte interphase (SEI) layers. Thus, the choice of electrolyte plays a critical role in improving battery stability and performance. Ionic liquids (ILs) offer a promising pathway to improved performance owing to their high thermal and electrochemical stability and excellent ionic conductivity. In this work, we employ density functional theory (DFT) and ab initio molecular dynamics (AIMD) simulations to gain atomistic insights into SEI formation and stability by investigating the interactions of the IL containing N,N-methylpropylpyrrolidinium (PYR13 +) cation, bis-(fluorosulfonyl)-amide (FSI-) and bis-(trifluoromethylsulfonyl)-amide (TFSI-) anions (PYR13FSI and PYR13TFSI), along with sodium salts NaFSI and NaTFSI, with the Na(110) metallic surface. Detailed geometric and electronic structure analyses capture the anode/electrolyte interfacial chemistry, encompassing both IL and salt interactions and their decomposition pathways to model the early stages of SEI formation. Our results show that FSI- interacts more strongly than TFSI- and undergoes spontaneous dissociation upon structural relaxation, whereas PYR13 + and TFSI- remain intact. AIMD trajectories at 298 K over 5-10 ps reveal the formation of decomposition products, primarily NaF, which is known to contribute to SEI stabilization. Compared to FSI-, TFSI- exhibits delayed decomposition, and PYR13 + cation remains intact throughout. Overall, these findings unravel the distinct interfacial behaviors of FSI- and TFSI- and highlight the critical role of anion chemistry in governing SEI formation and stability in sodium metal batteries.

PMID 42553544
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PubMedAngewandte Chemie (International ed. in English)2026-08-05

In Situ Tracking of Radical Evolution in a Conjugated Covalent Organic Framework for Reversible Sodium Storage.

Ma Chunrong C, Wang Ting T, Zhang Fengling F, Zhang Xin X et al.

Covalent organic frameworks (COFs) have emerged as promising platforms for sodium-ion storage owing to their tunable redox-active sites and ordered porous architectures. However, the role of radical intermediates in their electrochemical processes remains elusive due to the lack of direct experimental evidence. Herein, we report a highly crystalline β-ketoenamine-linked COF (BT-COF-AA) that delivers exceptional rate capability and ultralong cycling stability over 10 000 cycles at 5 A g- 1. More importantly, in situ electron paramagnetic resonance (EPR) spectroscopy provides time-resolved and direct observation of transient radical intermediates, enabling the elucidation of a sequential sodium-ion storage mechanism. Specifically, Na+ ions initially coordinate with nitrogen sites in benzothiadiazole units, triggering localized electron transfer and the formation of stabilized radicals. Subsequent sodiation occurs at carbonyl oxygen sites, generating ketyl radicals accompanied by dynamic electron delocalization across the conjugated framework. This reversible radical evolution establishes a framework-coupled redox pathway that underpins the outstanding electrochemical performance. Combined experimental and theoretical results reveal a radical-mediated charge storage mechanism and provide fundamental insights for the rational design of high-performance organic electrode materials.

PMID 42554430
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