2023
DOI: 10.3390/ph16010072
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Stability Study of Parenteral N-Acetylcysteine, and Chemical Inhibition of Its Dimerization

Abstract: Parenteral N-acetylcysteine has a wide variety of clinical applications, but its use can be limited by a poor chemical stability. We managed to control parenteral N-acetylcysteine stability, and to study the influence of additives on the decrease of N-acetylcysteine degradation. First, an HPLC-UV dosing method of N-acetylcysteine and its main degradation product, a dimer, was validated and the stability without additive was studied. Then, the influence of several additives (ascorbic acid, sodium edetate, tocop… Show more

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Cited by 4 publications
(3 citation statements)
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“…Extending the scope beyond the aforementioned substrates, the protocol effectively facilitated the conversion of ploy-aromatic (2u) and heteroaromatic (2v and 2w) thiols into their respective disulfides. To underscore the practical utility of this approach, we have employed it in the oxidation of bioactive thiols, namely N-(tert-butoxycarbonyl)-L-cysteine methyl ester 1x and N-acetyl-L-cystine 1y (Figure 3), which have been used as treatments for acute paracetamol toxicity and peptide synthesis, respectively [35,36]. This resulted in the formation of the corresponding disulfides 2x and 2y in 66% and 98% yields, respectively.…”
Section: Resultsmentioning
confidence: 99%
“…Extending the scope beyond the aforementioned substrates, the protocol effectively facilitated the conversion of ploy-aromatic (2u) and heteroaromatic (2v and 2w) thiols into their respective disulfides. To underscore the practical utility of this approach, we have employed it in the oxidation of bioactive thiols, namely N-(tert-butoxycarbonyl)-L-cysteine methyl ester 1x and N-acetyl-L-cystine 1y (Figure 3), which have been used as treatments for acute paracetamol toxicity and peptide synthesis, respectively [35,36]. This resulted in the formation of the corresponding disulfides 2x and 2y in 66% and 98% yields, respectively.…”
Section: Resultsmentioning
confidence: 99%
“…The data showed that NAC was stable for 420 days when stored at 2–8, 18–25 and 40°C (To et al, 2008). Stability of parenteral dosage forms of NAC was evaluated at 25 ± 2°C and under refrigeration conditions (5 ± 3°C) for 8 days (Primas et al, 2023). The results showed that 25 mg/ml NAC, diluted with 5% dextrose in water and placed in a polymeric Viaflo® bag, was stable for 24 h at room temperature and 4 days under refrigeration conditions.…”
Section: Discussionmentioning
confidence: 99%
“…The data showed that NAC was stable for 420 days when stored at 2-8, 18-25 and 40 C (To et al, 2008). Stability of parenteral dosage forms of NAC was evaluated at 25 ± 2 C and under refrigeration conditions (5 ± 3 C) for 8 days (Primas et al, 2023). The results…”
Section: Calibration Curvesmentioning
confidence: 99%