Abstract

The nasal route of drug administration, as is well known, is characterized by some advantages: absorption rate and rapid onset of therapeutic effect, availability of drug delivery without hepatic first-pass elimination, it is suitable and easily accessible. Earlier a medication for nasal administration with noopept – a low toxic substance with peptide nature without any side effects and high activity has been developed.After advance investigations, a solution of sodium carboxymethylcellulose providing the highest rate of noopept releasing was chosen as a delivery base.The aim of work the study of surfactants' influence on the noopept releasing from the nasal dosage form.Materials and methods. For the investigation, the compositions containing twin-80 from 0 % to 3 % were prepared. Surfactant was added to the nasal dosage form containing noonpept 1 %, glycerol, and bishofit poltavsky equally by 5 % and solution of sodium carboxymethylcellulose. Noopept releasing was studied using the method of equilibrium dialysis by Kruvchinsky through the semipermeable membrane – cellophane film “Kuprofan” after 30 minutes. Noopept concentration was determined by the UV-spectrophotometry at 258 nm. Results. Results of investigation have verified that the addition of twin-80 to nasal dosage form with noopept provides with a better level of releasing of the active substance. At the same time, increasing of concentration more than 1 % hasn’t a significant influence on the noopept releasing.Conclusions. It was determined that the content of twin-80 has a significant influence on a noopept releasing from the nasal dosage forms. The concentration of twin-80 1 % provides optimal releasing.

Highlights

  • Після попередніх досліджень як основу-носій обрали розчин натрій карбоксиметилцелюлози, який забезпечував найвищі показники вивільнення ноопепту

  • Surfactant was added to the nasal dosage form containing noonpept 1 %, glycerol, and bishofit poltavsky by 5 % and solution of sodium carboxymethylcellulose

  • Noopept releasing was studied using the method of equilibrium dialysis by Kruvchinsky through the semipermeable membrane – cellophane film “Kuprofan” after 30 minutes

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Summary

Introduction

Після попередніх досліджень як основу-носій обрали розчин натрій карбоксиметилцелюлози, який забезпечував найвищі показники вивільнення ноопепту. До складу назальних лікарських форм для підвищення біодоступності можливе додавання речовин – енхансерів абсорбції. Поверхнево-активну речовину додавали до складу назальної лікарської форми, що містить 1 % ноопепту, по 5 % гліцерину та бішофіту полтавського та розчин натрій карбоксиметилцелюлози. Додавання твіну-80 до назальної лікарської форми з ноопептом забезпечує кращий рівень вивільнення діючої речовини. Що вміст твіну-80 чинить значущий вплив на вивільнення ноопепту з назальної лікарської форми. The nasal route of drug administration, as is well known, is characterized by some advantages: absorption rate and rapid onset of therapeutic effect, availability of drug delivery without hepatic first-pass elimination, it is suitable and accessible. Earlier a medication for nasal administration with noopept – a low toxic substance with peptide nature without any side effects and high activity has been developed

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