The substantiation of the method for introduction of lysozyme hydrochloride and ascorbic acid in the composition of the medicated chewing gum “Lysodent C”

Authors

DOI:

https://doi.org/10.24959/ubphj.19.228

Keywords:

medicated chewing gums “Lysodent С”, lysozyme hydrochloride, ascorbic acid, chewable base Health in Gum® brand PWD-01, physico-chemical and pharmacotechnological studies

Abstract

Topicality. In recent years, medicated chewing gums have been widely distributed as a drug delivery system.
The Industrial Technology of Drugs Department of NUPh develops compressed chewing gums under the conventional name “Lysodent C” for the prevention and treatment of dental diseases, in which as active pharmaceutical ingredients ascorbic acid and lysozyme hydrochloride are used, and as a chewable base – composition Health in Gum® of brand PWD-01 (Cafosa, Spain).
Aim. To study the physico-chemical and pharmacotechnological properties of active pharmaceutical ingredients and chewable base for the purpose of establishing a method for the introduction of lysozyme hydrochloride and ascorbic acid into the composition of the compressed medicated chewing gums “Lysodent C”.
Materials and methods. Research objects: lysozyme hydrochloride, ascorbic acid, Health in Gum® of brand PWD-01 and mixture thereof. During the experiment, the physico-chemical (moisture absorption) and pharmacotechnological (optical microscopy, flowability, bulk density and tap-density, determination of granulometric composition by analytical sifting) of the substances’ powders methods were used in accordance with the requirements of SPU 2.0.
Results and discussion. The crystallographic and sieve analysis showed the polydispersity and polymorphism of
the particles of active pharmaceutical ingredients mixture and its combination with the chewing gum base, indicating
a possible stratification of the samples under study in the process of a solid dosage form obtaining. Study of the substances’ moisture absorption capacity has shown non-hygroscopicity of ascorbic acid and hygroscopicity of lysozyme hydrochloride and chewable base, which, in turn, indicates the need for the introduction of moisture absorbing agents to the composition of medicated chewing gums or maintenance of 40 % relative humidity of the environment in the production of the chewing gums. According to the results of pharmacotechnological studies, the substance of ascorbic acid has a satisfactory flowability, the composition of HiG brand PWD-01 has good flowability, and lysozyme hydrochloride – acceptable flowability, which accordingly provides for the adjustment of this indicator.
Conclusions. Based on the studies conducted, it has been determined that the rational way of lysozyme hydrochloride administering to the composition of medicated chewing gums using pre-granulation technology, and ascorbic acid by premixing
with lysozyme granulate and chewable base to avoid oxidation of the substance at contact with the moisturizer.

Author Biographies

Yu. S. Maslii, National University of Pharmacy

Candidate of Pharmaceutical Sciences, assistant professor of the Department of Industrial Technology of Drugs

O. A. Ruban, National University of Pharmacy

Doctor of Pharmacy, professor, head of the Department of Industrial Technology of Drugs

T. E. Kolisnyk, National University of Pharmacy

postgraduate student of the Department of Industrial Technology of Drugs

O. A. Liapunova, National University of Pharmacy

Candidate of Pharmaceutical Sciences, assistant professor of the Department of Industrial Pharmacy

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Published

2019-09-02

Issue

Section

Biopharmaceutical research