Abstract

The problem of drug-resistant tuberculosis treatment is complex and urgent: the standard of treatment includes the oral administration of six names of antibiotics, i.e. up to twenty tablets a day by the patient. This causes severe side effects, including those appeared due to the formation of toxic products of drug interactions in the body. Therefore, it is important that some drugs dissolve in a stomach, and others – in the intestine, which will lead to increased bioavailability, reduced dosage and toxicity. The development of targeted delivery systems for drugs with controlled release, targeted delivery and minimization of side effects are of interest. One of the promising methods is polyelectrolytic multilayers and the technology of creating such layers by a step-by-step adsorption of heterogeneously charged polyelectrolytes. The aim of this article is the microencapsulation of anti-tuberculous drugs into biopolymers coated with polyelectrolytic multilayers, and the solubility study of microcapsules at pH values simulating various parts of the gastrointestinal tract. Materials and methods . Drugs as isoniazide, pyrazinamide, moxifloxacin, and biopolymers: gellan, pectin and sodium alginate, chitosan and dextran sulfate, as well as Eudragit S are used to prepare microcapsules. The obtained microcapsules are studied by a method of scanning electron microscopy. Quantitative determination of the effectiveness of the inclusion of drugs in microcapsules was carried out using pharmacopoeial methods. Results and discussion. The inclusion efficiency rises with an increase of biopolymer concentration. The inclusion efficiency increases in the row isoniazide <pyrazinamide <moxifloxacin. The possibility of microencapsulation of anti-tuberculosis drugs of pyrazinamide, isoniazide and moxifloxacin by means of coating with polyelectrolytic multilayers is shown. At pH = 7.4, the degree of release of the drugs from microcapsules without applied multilayers for 12 hours was more than 80%, i.e. the prolongation was 12 hours. In the case of microcapsules coated with polyelectrolytic multilayers: for 12 hours – 55/50%, for 18 hours – more than 87/80%. Conclusion . The possibility of preparation of microcapsules of anti-tuberculosis drugs using biopolymers coated with polyelectrolytic layers, having a prolonged action is up to 18 hours, i1.5 times greater than that without coating.

Highlights

  • The problem of drug resistant tuberculosis treatment (DR-TB) is difficult and timely

  • The aim of this article is the microencapsulation of anti-tuberculous drugs into biopolymers coated with polyelectrolytic multilayers, and the solubility study of microcapsules at pH values simulating various parts of the gastrointestinal tract

  • The aim of this work is the encapsulation of anti-tuberculosis drugs in the biopolymers coated with polyelectrolytic multilayers, and evaluation of drug release at values рН, modeling various sites of a gastrointestinal tract

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Summary

Introduction

The problem of drug resistant tuberculosis treatment (DR-TB) is difficult and timely. The standard of treatment of DR-TB has provided reception of 6 antibiotics by the patient, i.e. 20 tablets each day. It causes heavy side effects because of the formation of toxic products in organism as a result of drugs interaction. It is important that some drugs were dissolved in a gastric, and others were soaked up in intestines that lead to the increase of bioavailability, reduction of a dosage, and decrease in toxicity [1]. As a model of antituberculosis drug rifampicin has been more studied [5,6,7,8, 11,12]

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