Comparison of the rate of release of active substances from solutions of hydroxymethylpropyl cellulose and hydroxyethyl cellulose for selecting the optimal polymer for the development of ear drops


如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅或者付费存取

详细

Drops are a liquid dosage form, which can go out of target place, so the use of a substance that gives the drops viscosity which prevents solution of drops to go out of place of applications, as polymers which are very important but that use may effect on release of active ingredients in drops, so in this study we studied the effect of used HPMC which is polymer used for viscoelastic, as well as an excipient and controlled-delivery component in ear drops. The aim of the work was to compare the rate of release of active substances from solutions of hydroxymethylpropyl cellulose and hy-droxyethyl cellulose, as the choice of the optimal polymer for the development of ear drops. We have studied the use of HPMC and HEC polymer for obtaining viscoelastic liquid dosage forms in the form of ear drops, as excipients that control the release. For the analysis, ofloxacin was chosen as active substances, in view of its high activity on microorganisms that cause otitis media, and HPMC and HEC, ethyl alcohol 96% and purified water were used as auxiliary substances in the analyzed compositions. To determine the viscosity of solutions, we have chosen a glass capillary viscometer VPZH-2, in accordance with the recommendation of the State Pharmaceutical Organization. The release was carried out by equilibrium dialysis through a semiper-meable membrane using a regenerated cellulose tubular membrane (model T3). The HPLC method was used to identify the active substance. In view of the data obtained on the release of the active substance, for the development of the composition and technology of ear drops, as an auxiliary component, we chose HPMC.

全文:

受限制的访问

作者简介

Balloul Ghadeer

Belgorod National Research University

编辑信件的主要联系方式.
Email: ghadeerballoul@gmail.com
Undergraduate, Department of Pharmaceutical Technology, Faculty of Pharmacy Belgorod, Russia

D. Martceva

Belgorod National Research University

Email: dianamartceva@mail.ru
Assistent, Department of Pharmaceutical Technology, Faculty of Pharmacy Belgorod, Russia

E. Zhilyakova

Belgorod National Research University

Email: ezhilyakova@bsu.edu.ru
Dr.Sc. (Pharm.), Professor, Department of Pharmaceutical Technology, Faculty of Pharmacy Belgorod, Russia

N. Boyko

Peoples' Friendship University of Russia

Email: boykoniknik@gmail.com
Dr.Sc. (Pharm.), Associate Professor, Department of Pharmaceutical Technology, Faculty of Pharmacy Belgorod, Russia

A. Abdulhadi

Belgorod National Research University

Email: hadibm@icloud.com
Post-graduate Student, Department of Pharmaceutical Technology, Faculty of Pharmacy Belgorod, Russia

Mahmoud Wissam

Belgorod National Research University

Email: wissam.pharma@gmail.com
Post-graduate Student, Department of Pharmaceutical Technology, Faculty of Pharmacy Belgorod, Russia

参考

  1. Общая фармакопейная статья, ОФС.1.4.1.0011.15 Растворы (Obshhaja farmakopejnaja stat'ja, OFS. 1.4.1.0011.15 Rastvory).
  2. Pahuja P., Arora S., Pawar P. Ocular drug delivery system: a reference to natural polymers. Expert Opinion on Drug Delivery. 2012; 9(7): 837-861.
  3. Tangri P., Khurana S. Basics of ocular drug delivery systems.International Journal of Research in Pharmaceutical and Biomedical Sciences. 2011; 2(4): 1541-1552.
  4. Fu Y., Kao W.J. Drug release kinetics and transport mechanisms of non-degradable and degradable polymeric delivery systems. Expert Opin Drug Deliv. 2010; 7(4): 429-444. doi: 10.1517/17425241003602259.
  5. Son G.H., Lee B.J., Cho C.W. Mechanisms of drug release from advanced drug formulations such as polymeric-based drug-delivery systems and lipid nanoparticles. Journal of Pharmaceutical Investigation. 2017; 47: 287-296. https://doi.org/10.1007/s40005-017-0320-1.
  6. Fuller C.S., Mac Rae R.J., Walther M., Cameron R.E.Interactions in poly (ethylene oxide) - hydroxypropyl methyl-cellulose blends. Polymer. 2001; 42(23): 9583-9592.
  7. Liechty W.B., Kryscio D.R., Slaughter B.V., Peppas N.A. Polymers for drug delivery systems. Annu Rev Chem Biomol Eng. 2010; 1: 149-173. doi: 10.1146/annurev-chembioeng-073009-100847.
  8. Pekel N., Yoshi F., Kurve T., Guuven O. Radiation crosslinking of biodegradable hydroxypropylmethylcellulose. Carbo-hydr. Polym. 2004; 55(2): 139-147.
  9. Rowe R.C., Sheskey P.J., Owen S.C. Handbook of Pharmaceutical Excipients. 5th ed Pharmaceutical Press; American Pharmacists Association; Grayslake, IL: Washington, D.C.: 2005. p. 850.
  10. Takka S., Rajbhandari S., Sakr A. Effect of anionic polymers on the release rate of Propronolol Hydrochloride from matrix tablets. Eur. J.Pharm. Biopharm. 2001; 52: 75-82.
  11. Государственная фармакопея РФ 14-е изд. 2018. Часть 4. 1814 с. (Gosudarstvennaja farmakopeja RF 14-e izd. 2018. Chast' 4. 1814 s.).

补充文件

附件文件
动作
1. JATS XML
2. Fig. 1. Results of the release of ofloxacin from solutions of GPMC and GEC in the form of ear drops using HPLC

下载 (22KB)
3. Fig. 2. Chromatogram of a model solution of ear drops at six time points of ofloxacin

下载 (50KB)

版权所有 © Russkiy Vrach Publishing House, 2022
##common.cookie##