STUDY OF THE EFFECT OF MODIFIED AMINOALDEHYDE OLIGOMER WITH COLLAGEN

ИЗУЧЕНИЕ ДЕЙСТВИЯ МОДИФИЦИРОВАННОГО АМИНОАЛЬДЕГИДНОГО ОЛИГОМЕРА С КОЛЛАГЕНОМ
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Murodova Z., Akhmedov V.N., Olimov B.B. STUDY OF THE EFFECT OF MODIFIED AMINOALDEHYDE OLIGOMER WITH COLLAGEN // Universum: технические науки : электрон. научн. журн. 2024. 3(120). URL: https://7universum.com/ru/tech/archive/item/17029 (дата обращения: 04.05.2024).
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DOI - 10.32743/UniTech.2024.120.3.17029

 

АННОТАЦИЯ

В данной статье представлена информация о модификации коллагена модифицированным аминоальдегидом. Также приведены сведения о силах Ван-дер-Ваальса между этими молекулами. Чтобы приписать олигомерам различные свойства, необходимо знание их молекулярных свойств. По этой причине изучались строение олигомеров и взаимодействия между молекулами в них.

ABSTRACT

This article provides information on the modification of collagen with modified aminoaldehyde. Information is also given about Van der Waals forces between these molecules. In order to assign different properties to oligomers, knowledge of their molecular properties is required. For this reason, the structure of oligomers and interactions between molecules in them were studied.

 

Ключевые слова: амидная связь, ковалентная связь, аминоальдегидные олигомеры, эффект Вандера-Валлса, полимер.

Keywords: amide bond, covalent bond, aminoaldehyde oligomers, Wan-der Walls effect, polymer

 

Introduction. Today, the demand for aminoaldehyde oligomers in the world is increasing in many other industries, such as wood processing, textiles, production of plastic masses, as well as tanning[1-5]. Its high physico-mechanical, as well as a number of technological, including thermal stability, adhesion properties have led to the further expansion of the areas where aminoaldehyde oligomers are used in recent years. The growing demands for new materials based on aminoaldehyde oligomers and the development of effective methods for studying the effect of the composition and functionality of these compounds on its properties are receiving great attention[6-9].

Materials and methods. When different molecules come close to each other, there is a certain amount of interaction between them. The reason for this effect is the coulomb interaction of the electron and nucleus of one molecule with the electron and nucleus of another molecule[10-14]. Synthesized oligomer binds with free functional groups in leather collagen by forming intermolecular hydrogen (Fig. 1) and chemical bonds (Fig. 2).

 

 

Figure 1. Intermolecular and hydrogen bonding formed by collagen oligomers

 

Figure 2. Mechanism of orientational Van der Waals effect

 

Results and discussion. Skin collagen with of the oligomer in order to analyze the formation of a mutual bond, it is necessary to have information about its composition and amount. Functional groups in collagen and their amount are shown in Table 1.

Table 1.

Type and number of functional groups in collagen

Functional groups

Meeting

100 g of collagen goods the number

Formula

Naming

carboxylic

 

Asparagine and glutamine acids

0.136

α - amino

lysine, oxylisine

0.037

guanidine

 

Arginine

0.055

Imide

 

 

Histidine

0.007

hydroxyl

Threonine, oxylisin

0.155

Amide

Amino - and imino acids and integrity

0.955

-

Proline, oxyproline

 

 

0.144

 

Regarding which functional groups of the oligomer synthesized with the functional groups in Table 1, there should be information about the reactivity of these functional groups. Table 2 provides information on what type of bond the functional groups form.

Table 2.

It reacts with collagens

Types

 

Connection harvest in being participation collagen groups

Covalent

 

 

Acidic (- COOH); basic ( -NH2,)

and non-dissociable hydroxyl ( -OH) groups

Electrovalent

Acidic (-COO - ) and  dissociable reasonable (- , )

 

Hydrogen

Peptide  groups (

Coordination

When dissociated acidic ( - COO-– and not dissociated in the case amino groups  

 

Based on the data presented in Tables-1, 2 above, we will study the interaction of the oligomer with collagen. Since skin collagen and synthesized oligomer composition is a polar macromolecule with a dipole moment by its nature, a dipole-dipole effect occurs, and this is an orientational intermolecular (Fig-3.) effect.

 

Figure 3. Chemical bonds formed by collagen with oligomers

 

In this case, the deformation of the electron cloud of the molecule is observed as a result of the effect of the poles. If one of these molecules were non-polar, we would have observed van der Waals induction , but here both molecules are polar. Dispersion Van der Waals effects occur between non-polar molecules, and this effect is not observed in the substances here.

Conclusion. As can be seen from the figure-1, 2, 3, the resulting intermolecular hydrogen bonds migrate due to breaking due to various external influences (due to the low energy of these bonds). However, due to the high energy of the chemical bond (which is formed between the hydroxyl and amino groups of the synthesized oligomer with the carboxyl of the aspartic acid residue in collagen), external mechanical effects are not enough to break it, and therefore migration is not observed. A clear example of this is the kinetics of degradation during thermal destruction of an oligomer-treated leather sample. It takes a lot of energy to break any chemical bond, which leads to an increase in the service life due to the fact that the leather is not observed during the service life and does not migrate.

 

References:

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  2.   Мурадова З. О. ИССЛЕДОВАНИЕ РАЦИОНАЛЬНОЙ ВНУТРЕННЕЙ ФОРМЫ ОБУВИ //Вестник магистратуры. – 2021. – №. 6-1 (117). – С. 11-12.
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  4. Энциклопедия полимеров / Ред. коллегия: В. А. Каргин (глав. ред.) [и др.] Т.1. – М.: «Советская энциклопедия», 1972. – 1224 с
  5. Аналитическая химия полимеров. / Под ред. Клайна Г..: Издательство иностранной литературы, 1963. С. 592.
  6. Гюнтер Райх. Коллаген. Изд-во Легкая индустрия, 1969, 239 стр
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  8. V.N. Axmedov, Z.Х. Rayimov, G.A. G‘afurova. Tereftal kislota hosilalari. – “Sharq-Buxoro” nashriyoti, Buxoro - 2022. – 152 bet.
  9. Shomurod N., Vokhid A., Bobir O. Preliminary quantum chemical analysis of synthesized monomers with the participation of vinylacetylene //International journal of progressive sciences and technologies. – 2020. – Т. 22. – №. 2. – С. 50-56.
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  12. Olimov B. B., Akhmedov V. N., Gafurova G. A. Application of derivatives of diatomic phenols as corrosion inhibitors //Euro Asian Conference on Analytical Research (Germany. – 2021. – Т. 15. – С. 136-138.
  13. Ахмедов В., Олимов Б., Гафурова Г. Винилацетилен иштирокида винил эфирлар олиш. НамДУ илмий ахборотномаси-Научный вестник НамГУ. – 2021.
  14. Bahodirovich, Olimov B., et al. "Synthesis of Resorcinol Vinyl Ether in the Mono-position, Influence of the Catalyst, Temperature and Solvent on the Reaction Yield." JournalNX, 2020, pp. 44-51.
Информация об авторах

Researcher of the Bukhara Institute of Engineering and Technology, Uzbekistan, Bukhara

соискатель Бухарского инженерно-технологического института, Узбекистан, г. Бухара

Cand. of tech. sciences, Professor of the Department of Chemistry Bukhara Engineering and Technology Institute, Republic of Uzbekistan, Bukhara

канд. тех. наук, проф. кафедры химии Бухарского инженерно-технологического института, Республика Узбекистан, г. Бухара

PhD, docent of the Department of Chemistry Bukhara Engineering and Technology Institute, Republic of Uzbekistan Bukhara

PhD, и.о. доц. кафедры химии Бухарского инженерно-технологического института, Республика Узбекистан, г. Бухара

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