Discrete optimization of the implementation stages of pharmaceutical development for a spray treatment for oral diseases

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Introduction. All over the world more than 3.5 billion people suffer from oral diseases, which can lead to endogenous infectious diseases and create conditions for external infections. The growing antimicrobial resistance of bacterial strains is a global health threat. Oligoalkyleneguanidine polymers may be promising compounds to solve this problem. The spray form for the application of these substances is the most optimal.

The aim of the study is to apply discrete optimization to implement the stages of pharmaceutical development of a spray based on branched oligohexamethyleneguanidine for the treatment of oral diseases.

Material and methods. Experiments are carried out using various equipment and samples with different compositions have been developed. The implementation of the pharmaceutical development stages was carried out using a discrete optimization algorithm.

Results. When implementing discrete optimization in pharmaceutical development, it is necessary to prioritize criteria and limitations using the target quality profile of the drug being developed. As a result of the optimization cycles carried out, the optimal composition was selected, which corresponds to the target quality profile, including such parameters as pH, dynamic viscosity, sterilizing filtration, adhesion of the formulations to the oral mucosa and the spray torch. A discrete optimization was carried out, taking into account the wetting edge angle and particle size distribution. The optimal composition was sample No. 8, which has pseudoplastic properties, provides unhindered spraying and prevents the composition from draining from the mucous membrane of the oral cavity.

Conclusion. During the study, the optimal ratio of components was determined and the development of a spray based on oligohexamethyleneguanidine with the implementation of stages of pharmaceutical development for discrete optimization was proposed.

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作者简介

D. Shatalov

MIREA – Russian Technological University

编辑信件的主要联系方式.
Email: shatalov_d@mirea.ru
ORCID iD: 0000-0003-4510-1721

Ph.D. (Pharm.)

俄罗斯联邦, Moscow

S. Kedik

MIREA – Russian Technological University

Email: shatalov_d@mirea.ru
ORCID iD: 0000-0003-2610-8493

Dr.Sc. (Tech.), Professor

俄罗斯联邦, Moscow

D. Akhmedova

MIREA – Russian Technological University

Email: shatalov_d@mirea.ru
ORCID iD: 0000-0002-0951-939X

Assistant

俄罗斯联邦, Moscow

A. Gromakova

All-Russian Scientific Research Institute of Medicinal and Aromatic Plants

Email: shatalov_d@mirea.ru
ORCID iD: 0000-0001-8984-0724

Dr.Sc. (Pharm), Chief Research Scientist

俄罗斯联邦, Moscow

Yu. Koroleva

MIREA – Russian Technological University

Email: shatalov_d@mirea.ru
ORCID iD: 0000-0001-8092-1990

Student

俄罗斯联邦, Moscow

A. Dolgovskaya

MIREA – Russian Technological University; Institute of Pharmaceutical Technologies

Email: shatalov_d@mirea.ru

Student

俄罗斯联邦, Moscow; Moscow

S. Kharchenko

MIREA – Russian Technological University

Email: shatalov_d@mirea.ru

Student

俄罗斯联邦, Moscow

D. Kirillova

MIREA – Russian Technological University

Email: shatalov_d@mirea.ru
ORCID iD: 0000-0002-3055-1116

Student

俄罗斯联邦, Moscow

D. Minenkov

Ishlinsky Institute for Problems in Mechanics of the Russian Academy of Sciences

Email: shatalov_d@mirea.ru
ORCID iD: 0000-0001-6432-8134

Senior Research Scientist

俄罗斯联邦, Moscow

A. Nikulin

MIREA – Russian Technological University

Email: shatalov_d@mirea.ru
ORCID iD: 0009-0004-2755-2734

Associate Professor

俄罗斯联邦, Moscow

参考

  1. Global oral health status report: towards universal health coverage for oral health by 2030. Geneva: World Health Organization; 2022. Licence: CC BY-NC-SA 3.0 IGO.
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  4. Shatalov D.O., Kedik S.A., Zhavoronok E.S. i dr. Opyt i perspektivy razvitija ispol'zovanija sinteticheskih antimikrobnyh veshhestv. Vse materialy. Jenciklopedicheskij spravochnik, 2016; 8: 14.
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  7. Shatalov D.O., Kedik S.A., Ajdakova A.V. i dr. Sovremennye podhody k razrabotke gotovyh lekarstvennyh form dlja lechenija zabolevanij polosti rta (obzor). Biofarmacevticheskij zhurnal. 2019; 11; 4; 15–28.
  8. Shatalov D.O, Kedik S.A., Krupenchenkova N.V., et al. Acute Toxicity of the Pharmaceutical Substance Branched Oligohexamethyleneguanidine Hydrochloride at Mice and Rats after Intragastric Administration. American Journal of Biomedical Science & Research. 2019; 4(2): 76–77.
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2. Fig. 1. Algorithmic sequence of R&D implementation

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3. Fig. 2. Viscosity values of samples obtained from viscosity-velocity curves

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4. Fig. 3. Viscosity-velocity flow curves of the test samples (а–е)

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5. Fig. 4. A typical view of a drop of the studied compositions on test substrates of various nature

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6. Fig. 5. Static prints of spray torches of samples No. 6, No. 3 and No. 8, respectively

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7. Fig. 6. Differential distribution of sprayed spray particles of experimental samples (compositions) by size

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