Effect of natural solubilizers on the solubility and dissolution of Aceclofenac By A. A. Osman*,, M. M. Nafadi.*, and N. D. Mortada** Department of Pharmaceutics,

Slides:



Advertisements
Similar presentations
In this study report the results of the effect of pH on the solubility of Nimesulide (BCS poorly soluble drug) in physiological pH. Some drugs having poor.
Advertisements

Unit 7: Solutions Properties of Solutions Presentation.
Pharmtech Contract Services Offered by the Division of Pharmaceutical Technology.
EFFECT OF PHYSICAL MODIFICATION AND IONIC STRENGTH ON THE SOLUBILITY AND DISSOLUTION OF PARACETAMOL By M.M.Nafadi From Department of Pharmaceutics and.
FORMULATION OF A FAST-DISSOLVING KETOPROFEN LYOPHILIZED TABLET
EFFECT OF FORMULATION FACTORS ON THE FLOATING SUSTAINED RELEASE PROPRANOLOL HYDROCHLORIDE CAPSULES M.M. Nafadi From Department of Pharmaceutics and Industrial.
Results and Discussion By: Victor, Eduard and David.
0 Nour S. A.; Nafadi M. M. and Abd-El Malak N. S. Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Cairo University, Cairo, Egypt.
Aim of work The main objective of this investigation was to optimize the formulation of chitosan beads with Ketorolac tromethamine to minimize the gastrointestinal.
Enhancement of Dissolution and Release Rate of Piroxicam From Witepsol W35 Suppository Base Using Lyophilized Inclusion Adduct of Piroxicam With Skimmed.
A Pharmaceutical Study on Felodipine “Enhanced Dissolution Characteristics of Felodipine” Ahmed Abd-El Bary, Mohamed M. Nafady,Mahmoud E. Nasr Department.
Solubility and Dissolution Pharmaceutical Technology.
PHYSICAL PROPERTIES OF ORGANIC COMPOUNDS Mr. Maywan Hariono.
Micro-Emulsion Xiaowen Feng Peking University, Department of Chemistry.
Quality by Design Application of Pharmaceutical QbD for Enhancement of the Solubility and Dissolution of a Class II BCS Drug using Polymeric Surfactants.
Curcumin, the constituent of Curcuma longa, is considered a very promising anticancer agent due to its potent and pleiotropic antineoplastic activity and.
PHARMACEUTICS- IV (PHT 414 ) Dr. Shahid Jamil SALMAN BIN ABDUL AZIZ UNIVERSITY COLLEGE OF PHARMACY L /9/2015 Factors Affecting Drug Absorption (Dosage.
A DONE BY: RONO KIPROTICH VICTOR U29/28970/2009 A COMPARATIVE STUDY ON DISSOLUTION PROFILES OF AMOXICILLIN IN AMOXICILLIN CONTAINING CAPSULES AVAILABLE.
Improving solubility and cellular absorption of Paclitaxel with solid lipid nanoparticles and cyclodextrin Jong-Suep Baek, Jae-Woo So, Ji-Sook Hwang, Cheong-Weon.
Micelle A micelle (rarely micella, plural micellae) is an aggregate of surfactant molecules dispersed in a liquid colloid. A typical micelle in aqueous.
Concentration.
Pharmaceutica 2015 Dubai 16th April 2015
Formulation factors By Dr. A. S. Adebayo.
Mastic is a well-known natural resin from the trunk and branches, of Pistacia lentiscus var. chia (Anacardiaceae), which is grown as endemic only in the.
Solutions Chapter 13 & 14. Solution  A uniform mixture that may contain solids, liquids, or gases  Also called a homogeneous mixture  Composed of a.
A Parmaceutical Study on Felodipine(Preparation and evaluation of Felodipine Therapeutic Transdermal system) Ahmed Abd El-Bary, Mohamed M. Nafady, Mahmoud.
h C1 Cd Cr C2 Donor Receiver K Permeable membrane D C0 Blood Donor
Copyright © by Holt, Rinehart and Winston. All rights reserved. ResourcesChapter menu Solutions You know from experience that sugar dissolves in water.
The Biopharmaceutical Classification System (BCS)
Liquisolid drug delivery system
Solubility Chapter 17 & 18. Solutions  Solutions are made of a solute and a solvent.  In this chapter we are concentrating on solutions of water. 
Bioavailability of Dietary Supplements: Key Issues in Defining the Research Agenda Impact of Formulation on Bioavailability? Discussion Leader: Stephen.
Advantages and disadvantages of solutions
Uday Khandavilli, PhD student, School of Chemistry, University College Cork, Cork 1.
學生 : 陳雅貞 日期 : Introduction Polycyclic aromatic hydrocarbons (PAHs) are pollutants of major concern in soils and sediments. Surfactant-enhanced.
An investigation into the stability and solubility of amorphous solid dispersion of BCS class II drugs Shrawan Baghel, WIT.
Characterization of the interaction between Lomefloxacin and Certain Gastro-retentive Polymers Amir Ibrahim Mohamed a, Osama A. A. Ahmed b, Amira Osama.
DEVELOPMENT, OPTIMIZATION AND PROCESS VALIDATION OF THE MODIFIED QUASSI EMULSION SOLVENT DIFFUSION METHOD FOR THE PREPARATION OF MICROSPONGES Rishabh Srivastava*,
Dispersed Systems. Dispersed system:  It is liquid preparations containing undissolved or immiscible drug distributed throughout a vehicle.  The substance.
CELECOXIB (BCS CLASS II MODEL DRUG) SOLUBILITY ENHANCEMENT BY CYCLODEXTRIN COMPLEXATION. Abhishek Juluri 1,Carmen Popescu 2, Prashanth Manda 1, Leon Zhou.
PITAVASTATIN CONTAINING NANOEMULSIONS:
- Pharmaceutical Equivalence Study
The Biopharmaceutical Classification System (BCS)
RESULTS CONCLUSIONS REFERENCES
Figure 6.2 Solution pH as a function of concentration for an acidic salt.
DRUG SOLUBILITY TECHNIQUES
Introduction Objective Experimental Results and Discussion
FORMULATION AND IN VITRO EVALUATION OF ATORVASTATIN SOLID DISPERSION
Chapter 12 Solutions.
Hashem Alsaab*, Rami M. alzhrani, Sai HS. Boddu
Investigations of the mechanisms of absorption of lycopene from the gastro-intestinal tract of the rat. Faisal W., O'Driscoll C. M. and Griffin B. T.1.
Solubility and Dissolution
Naofumi Hashimoto, Ph.D. Faculty of Pharmaceutical Sciences
Self emulsifying Drug Delivery System : Formulation
Microemulsion In Drug Delivery Systems
Non-electrolytes ‘Concentration expression
Pharmaceutical Technology I
J.Preethi*, P. Madhu, K. Arshad Ahmed Khan.
5. EXPERIMENT Material: Instrument Experiment condition:
Unit 13. Solutions (including Molarity)
Mansi K. Shah August 16, 2015 Drug Delivery Summit, Houston
Unit 12. Solutions (including Molarity)
Biopharmaceutics 4th year
Hemin J Majeed MSc. Pharmaceutical sciences
Hemin J Majeed MSc. Pharmaceutical sciences
Chapter 12 Solutions.
Formulation factors By Dr. A. S. Adebayo.
Level I Students (Fall Semester 2018/2019) General Chemistry (PC101)
Dr. Basavaraj K. Nanjwade M. Pharm, PhD. Department of Pharmaceutics
Presentation transcript:

Effect of natural solubilizers on the solubility and dissolution of Aceclofenac By A. A. Osman*,, M. M. Nafadi.*, and N. D. Mortada** Department of Pharmaceutics, Faculty of Pharmacy, Cairo University* and Ain Shams University**

Aim of work In this work, attempts were made to enhance the solubility of the poorly soluble Aceclofenac and hence its bioavailability. To accomplish this work, Aceclofenac solid dispersions were prepared using the gall bladder contents of three species from three different animal classes, namely: Fishes, Aves and Mammalia(Tilabia nilotica, hen and rabbit) ) respectively as well as synthetic solubilizers.

The prepared solid dispersions were subjected to surface tension measurements, solubility and dissolution studies. Any interactions between the drug and the used solubilizers, if any, were studied using differential scanning calorimetry and infrared spectroscopy.

Conclusion 1- The results of this work revealed that the used micellar system enhanced the solubility of the drug as well as its dissolution, especially in acid medium. The enhancement achieved by the natural solubilizers was comparable to that obtained by the synthetic solubilizer polysorbate 80.In this respect, the enhancement due to the biles of both hen and fish was superior to that of the rabbit.

2-These findings would rationalize the use of such natural substances as promising additives for the development of optimal formulation conditions of poorly water soluble drugs.

Solubility study

Dissolution Study

Table 1. Surface tension of aqueous solutions of Aceclofenac solid dispersions prepared with different solubilizers at 25±0.5 o C Surface tension (mN) Solubilizer L/SDC SDCSLSTween 80 Rabbit bile Fish bile Hen bile concentration w/w%