The Degradation Chemistry of GSK2879552: Salt Selection and Microenvironmental pH Modulation to Stabilize a Cyclopropyl Amine

2019 ◽  
Vol 108 (9) ◽  
pp. 2858-2864
Author(s):  
John M. Campbell ◽  
Mei Lee ◽  
Jacalyn Clawson ◽  
Sonya Kennedy-Gabb ◽  
Sarah Bethune ◽  
...  
Molecules ◽  
2018 ◽  
Vol 23 (7) ◽  
pp. 1719 ◽  
Author(s):  
Deepak Gupta ◽  
Deepak Bhatia ◽  
Vivek Dave ◽  
Vijaykumar Sutariya ◽  
Sheeba Varghese Gupta

The physicochemical and biological properties of active pharmaceutical ingredients (APIs) are greatly affected by their salt forms. The choice of a particular salt formulation is based on numerous factors such as API chemistry, intended dosage form, pharmacokinetics, and pharmacodynamics. The appropriate salt can improve the overall therapeutic and pharmaceutical effects of an API. However, the incorrect salt form can have the opposite effect, and can be quite detrimental for overall drug development. This review summarizes several criteria for choosing the appropriate salt forms, along with the effects of salt forms on the pharmaceutical properties of APIs. In addition to a comprehensive review of the selection criteria, this review also gives a brief historic perspective of the salt selection processes.


2019 ◽  
Vol 7 (18) ◽  
pp. 2915-2919 ◽  
Author(s):  
Weike Chen ◽  
Shuxin Li ◽  
Paul Renick ◽  
Su Yang ◽  
Nikhil Pandy ◽  
...  

A soluble, supramolecular peptide serves as an antimicrobial depot to release activated peptides in response to microenvironmental pH change around bacteria.


2014 ◽  
Vol 58 (11) ◽  
pp. 6385-6397 ◽  
Author(s):  
Wafi Siala ◽  
Marie-Paule Mingeot-Leclercq ◽  
Paul M. Tulkens ◽  
Marie Hallin ◽  
Olivier Denis ◽  
...  

ABSTRACTBiofilm-related infections remain a scourge. In anin vitromodel of biofilms usingStaphylococcus aureusreference strains, delafloxacin and daptomycin were found to be the most active among the antibiotics from 8 different pharmacological classes (J. Bauer, W. Siala, P. M. Tulkens, and F. Van Bambeke, Antimicrob. Agents Chemother. 57:2726–2737, 2013, doi:10.1128/AAC.00181-13). In this study, we compared delafloxacin to daptomycin and vancomycin using biofilms produced by 7 clinical strains (S. aureusepidemic clones CC5 and CC8) in order to rationalize the differences observed between the antibiotics and strains. The effects of the antibiotics on bacterial viability (resazurin reduction assay) and biomass (crystal violet staining) were measured and correlated with the proportion of polysaccharides in the matrix, the local microenvironmental pH (micro-pH), and the antibiotic penetration in the biofilm. At clinically meaningful concentrations, delafloxacin, daptomycin, and vancomycin caused a ≥25% reduction in viability against the biofilms formed by 5, 4, and 3 strains, respectively. The antibiotic penetration within the biofilms ranged from 0.6 to 52% for delafloxacin, 0.2 to 10% for daptomycin, and 0.2 to 1% for vancomycin; for delafloxacin, this was inversely related to the polysaccharide proportion in the matrix. Six biofilms were acidic, explaining the high potency of delafloxacin (lower MICs at acidic pH). Norspermidine and norspermine (disassembling the biofilm matrix) drastically increased delafloxacin potency and efficacy (50% reduction in viability for 6 biofilms at clinically meaningful concentrations) in direct correlation with its increased penetration within the biofilm, while they only modestly improved daptomycin efficacy (50% reduction in viability for 2 biofilms) and penetration, and they showed marginal effects with vancomycin. Delafloxacin potency and efficacy against biofilms are benefited by its penetration into the matrix and the local acidic micro-pH.


2000 ◽  
Vol 4 (5) ◽  
pp. 427-435 ◽  
Author(s):  
Richard J. Bastin ◽  
Michael J. Bowker ◽  
Bryan J. Slater

2012 ◽  
Vol 434 (1-2) ◽  
pp. 148-154 ◽  
Author(s):  
Chika Taniguchi ◽  
Ryo Inoue ◽  
Yohei Kawabata ◽  
Kazuhiro Yamashita ◽  
Koichi Wada ◽  
...  

RSC Advances ◽  
2016 ◽  
Vol 6 (109) ◽  
pp. 107310-107316
Author(s):  
Chunfei Hu ◽  
Yu-Sheng Lin ◽  
Hongmei Chen ◽  
Jingjing Liu ◽  
Fuqiang Nie

We proposed and demonstrated a concentration gradient generator (CGG) to resist H460 lung cancer cells using curcumin in microenvironmental pH conditions.


2012 ◽  
Vol 101 (8) ◽  
pp. 2777-2786 ◽  
Author(s):  
Mikolaj Milewski ◽  
Raghotham R. Pinninti ◽  
Audra L. Stinchcomb

2017 ◽  
Vol 36 (3) ◽  
pp. 207-219 ◽  
Author(s):  
Mausumee Guha ◽  
Linh Nguyen ◽  
Florence Poitout-Belissent ◽  
Agathe Bedard ◽  
Kavita Raman

Salt forms of pharmaceutical compounds can have unique pharmacokinetic and toxicity properties. MDV1634 was evaluated for neurology indication and also demonstrated blood pressure (BP)-lowering effects in nonclinical studies. During the chemistry manufacturing campaign, 2 salt forms, dihydrochloride (2HCl) and maleate (MAL), which improved chemical stability and water solubility of the free base were identified. MDV1634.MAL showed better chemical attributes and was evaluated in toxicology studies for further development. A 28-day oral toxicity study in dogs with MDV1634.MAL demonstrated partially reversible renal toxicity. Although MAL salt is generally regarded as safe, renal toxicity is sometimes observed in rats and dogs. To evaluate contribution of each salt form to renal toxicity and BP lowering, an additional 28-day study was conducted with MDV1634.2HCL and MDV1634.MAL, which included toxicokinetics, continuous BP measurement in a subset of dogs, and sensitive urinary biomarker evaluation for temporal monitorability and reversibility of potential renal findings. In the repeat study, both salt forms showed similar exposures during the dosing period, but renal tubular toxicity was observed only with MDV1634.MAL and not with MDV1634.2HCl. The renal findings with MDV1634.MAL included early urinary biomarker changes (increase in albumin, clusterin, β2 microglobulin, and neutrophil gelatinase-associated lipocalin); elevations in serum blood urea nitrogen and creatinine; and microscopic findings of partially reversible tubular basophilia, single cell necrosis, pigmentation, and mineralization. The renal findings in contrast to the BP findings were MAL-specific and considered not related to MDV1634, thereby under scoring the importance of salt forms in pharmaceutical development.


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