Abstract

<p align="center"><strong>Development of analitical procedures of quality control for labolatory baches of DEXTROSE CONTAINING solutions for peritoneal dialysis </strong></p><p> <strong>N. HUDZ</strong></p><p align="center"><em>Danylo Halytsky Lviv National Medical University</em><em>, Ukraine</em><em><br /> <br /> </em><strong></strong></p><p><strong>Summary</strong>. Laboratory batches are used in the initial stages of pharmaceutical development for the purpose of testing the proposed composition, techniques of quality control, studying features of a medicinal product, excipients impact on its physical and chemical characteristics and etc. Implementation methods of pharmacopoeia monographs of the European Pharmacopoeia for "Solutions for peritoneal dialysis" may be impossible in early stages due to unavailability of expensive analytical equipment or reagents at the site of the development. 5-hydroxymethylfurfural is a product of irreversible dextrose dehydratation. The method of direct spectrophotometric determination of 5-hydroxymethylfurfural is offered for dextrose containing solutions for peritoneal dialysis. Its concentration is calculated on the basis of molar absorption coefficient (16830 L∙mol<sup>-1</sup>∙cm<sup>-1</sup>). This technique enables in the early stages of pharmaceutical development to assess the effect of pH, dextrose, sodium lactate and sterilization on the degree of dextrose degradation in solutions for peritoneal dialysis. Direct argentometric method makes possible to quickly determine the content of chloride ions and establish the relationship between the amount of hydrochloric acid as stabilizer, pH, and content of chloride ions.</p><p><strong>Key words</strong>: peritoneal dialysis, argentometric method, 5-hydroxymethylfurfural</p><p><strong>Introduction.</strong> Peritoneal dialysis solutions are multicomponent systems which include incompatible composition: dextrose and sodium lactate. In the presence of latter dextrose is undergone degradation, the extent of which depends primarily on pH, concentration of sodium lactate and dextrose monohydrate, sterilization regime. Previous studies on the development of dextrosecontaining peritoneal solutions showed that the feature of their composition and technology was the selection of quantities of hydrochloric acid for optimal pH for sterilization to minimize the formation of dextrose degradation products (DDPs) during heat sterilization.</p><p>The purpose of this research is to evolve the available analytical procedures for the initial development of the laboratory technology of solutions for peritoneal dialysis (PD).</p><p><strong>Methods.</strong> We used the methods of analysis, synthesis, systematization, comparison, as well, argentometric, potentiometric, and spectrophotometric methods to reach the purpose and tasks of the research.</p><p><strong>Results and discussion</strong>. We offered the procedure of direct argentometric method for the assay of chloride ions and study of the effect of hydrochloric acid on their content at different pH of solutions (pH 5.2-6.6) (transfer 10.0 ml of Sample solution to a suitable container, add 0.8 ml of potassium chromate, and titrate with 0.1 M solution of silver nitrate. Each ml of 0.1 M solution of silver nitrate is equivalent to 3.545 mg of chloride ions (Cl<sup>-</sup>). Among the priorities in the development of this technique was selection of the volume of sample for analysis, calculation of the volume indicator, which is necessary for a clear color change, and evaluation of its suitability for routine analysis and prospective validation. Experimental data showed that the difference between the content of chloride ions in all the solutions at pH 5.2-6.6 was within the complete uncertainty of analysis (approximately ΔAs = 1,6 %).</p><p> The direct ultraviolet spectrophotometry method is offered for the determination of the main products of dextrose dehydratation (3,4-dideoxyglucosone-3-en and 5-hydroxymethylfurfural). According to experimental data, the wavelength of maximum absorption depends on the pH of the solution. The lower the pH value is, the more the maximum position is shifted to the right (at pH 5.2-6.6 there is maximum position at the range of 283-275 nm). This maximum is caused by forming 5-hydroxymethylfurfural after heat sterilization. With increasing pH from 5.2 to 6.6 absorption at the wavelength 228-230 nm gradually increases, which is consistent with literature data, that degradation process is dominant for 3,4-dideoxyglucosone-3-en at a pH above 3.5.</p><p><strong> Conclusions.</strong> The method of direct ultraviolet spectrophotometry with usage of molar absorption coefficient enables to measure 5-hydroxymethylfurfural as a major dextrose degradation product in solutions for peritoneal dialysis at the early stages of pharmaceutical development and to assess the effect of pH, dextrose, sodium lactate and sterilization treatment on the degree of dextrose degradation. Direct argentometric method makes possible to quickly measure the content of chloride ions and establish the relationship between the amount of hydrochloric acid as stabilizer, pH, and content of chloride ions.</p>

Highlights

  • laboratory batches are used in the initial stages of pharmaceutical development

  • Its concentarion is calculated on the basis of molar absorption coef cient

  • This technique enables in the early stages of pharmaceutical development to assess the effect

Read more

Summary

Introduction

Ця методика дає можливість на ранніх етапах фармацевтичної розробки оцінювати вплив рН, концентрації глюкози, натрію лактату і режиму стерилізації на ступінь деградації глюкози в перитонеальних діалізних розчинах. Інструментальні методи аналізу використовували для вимірювання рН розчинів до і після стерилізації, а також для знімання спектрів поглинання в ультрафіолетовій і видимій ділянці спектра, визначення максимумів поглинання, значення оптичної густини в максимумах поглинання і при певних довжинах хвиль. Для кількісного визначення хлорид-іонів та вивчення впливу хлористоводневої кислоти на їх вміст запропоновано методику прямого аргентометричного методу.

Results
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.