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Pharmaceutical compounds photolysis: pH influence.

ABSTRACT: The operating parameters of photolytic and photocatalytic reaction processes directly affect the efficiency in the degradation of compounds. In particular, pH is a variable that needs to be considered as it exerts great influence on adsorption, absorption, solubility, among others. This study describes the application of the photolytic process, at different pHs, in the degradation of different pharmaceutical compounds. Photolytic reactions were performed with the following contaminants: acetylsalicylic acid (ASA), ibuprofen (IBP) and paracetamol (PAR). In addition, a comparison was performed using the commercial catalyst P25. The results indicated a great influence of the pH in the kinetic constant of the photodegradation and in the UV absorbance of the species. In particular, the degradation of ASA and PAR were favored with the reduction of pH, while the degradation of IBU and SA were favored by increasing. Also, the chromatograms indicated that pH may affect the by-products formed. In comparison, the photocatalysis process in the presence of P25 proved to be much more effective, but it was not possible to achieve complete mineralization of the compounds.

SUBMITTER: Kounaris Fuziki ME

PROVIDER: S-EPMC9971040 | biostudies-literature | 2023 Feb

REPOSITORIES: biostudies-literature

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Pharmaceutical compounds photolysis: pH influence.

Kounaris Fuziki Maria Eduarda ME Ribas Laura S LS Tusset Angelo Marcelo AM Brackmann Rodrigo R Dos Santos Onelia A A OAA Lenzi Giane Gonçalves GG

Heliyon 20230211 2

The operating parameters of photolytic and photocatalytic reaction processes directly affect the efficiency in the degradation of compounds. In particular, pH is a variable that needs to be considered as it exerts great influence on adsorption, absorption, solubility, among others. This study describes the application of the photolytic process, at different pHs, in the degradation of different pharmaceutical compounds. Photolytic reactions were performed with the following contaminants: acetylsa ...[more]

PMID: 36865467

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Project description:In this work we report the effects of continuous UV-light (276 nm, ~2.20 W.m(-2)) excitation of human insulin on its absorption and fluorescence properties, structure and functionality. Continuous UV-excitation of the peptide hormone in solution leads to the progressive formation of tyrosine photo-product dityrosine, formed upon tyrosine radical cross-linkage. Absorbance, fluorescence emission and excitation data confirm dityrosine formation, leading to covalent insulin dimerization. Furthermore, UV-excitation of insulin induces disulphide bridge breakage. Near- and far-UV-CD spectroscopy shows that UV-excitation of insulin induces secondary and tertiary structure losses. In native insulin, the A and B chains are held together by two disulphide bridges. Disruption of either of these bonds is likely to affect insulin's structure. The UV-light induced structural changes impair its antibody binding capability and in vitro hormonal function. After 1.5 and 3.5 h of 276 nm excitation there is a 33.7% and 62.1% decrease in concentration of insulin recognized by guinea pig anti-insulin antibodies, respectively. Glucose uptake by human skeletal muscle cells decreases 61.7% when the cells are incubated with pre UV-illuminated insulin during 1.5 h. The observations presented in this work highlight the importance of protecting insulin and other drugs from UV-light exposure, which is of outmost relevance to the pharmaceutical industry. Several drug formulations containing insulin in hexameric, dimeric and monomeric forms can be exposed to natural and artificial UV-light during their production, packaging, storage or administration phases. We can estimate that direct long-term exposure of insulin to sunlight and common light sources for indoors lighting and UV-sterilization in industries can be sufficient to induce irreversible changes to human insulin structure. Routine fluorescence and absorption measurements in laboratory experiments may also induce changes in protein structure. Structural damage includes insulin dimerization via dityrosine cross-linking or disulphide bond disruption, which affects the hormone's structure and bioactivity.

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Pharmaceutical compounds photolysis: pH influence.

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Pharmaceutical compounds photolysis: pH influence.

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