Polymeric Eutectic System

2012 ◽  
Vol 528 ◽  
pp. 180-183 ◽  
Author(s):  
S. Tuntarawongsa ◽  
T. Phaechamud
Keyword(s):  
Surface Tension ◽  
Drug Release ◽  
Chemical Interaction ◽  
Polymer Concentration ◽  
Eutectic Mixture ◽  
Eutectic System ◽  
Biocompatible Polymer ◽  
Exponential Curve ◽  
Pharmaceutical Applications ◽  
The One

The liquid eutectic system comprising 1:1 menthol:camphor was selected to use as solvent due to it was lowest viscosity. Both menthol and camphor used in this eutectic system have been reported for their many pharmaceutical used. Various polymers were tested for their solubility in this eutectic system. Eudragit® EPO showed the highest solubility. Eudragit® EPO was the one of biocompatible polymer which could dissolve in this eutectic system up to 40% w/w with no chemical interaction of each compound. Viscosity of this system showed the exponential curve as a function of polymer concentration but all concentration showed the newtonian rheology. The pH and surface tension were slightly affected by type and amount of polymers. The obtained polymeric eutectic mixture should control the drug release for pharmaceutical applications.

Development of Rifampicin Nanoparticles by 32 Factorial Design

2010 ◽  
Vol 3 (3) ◽  
pp. 1085-1091
Author(s):  
Gambhire Makarand ◽  
Vaishali Gambhire ◽  
Bhalekar Mangesh
Keyword(s):  
Particle Size ◽  
Drug Release ◽  
Factorial Design ◽  
Chemical Interaction ◽  
Polymer Concentration ◽  
In Vitro Release ◽  
Entrapment Efficiency ◽  
Plga Nanoparticles ◽  
Sustained Drug Release ◽  
32 Factorial Design

The preparation and physico-chemical evaluation of rifam-picinloaded poly-(lactic-co-glycolic) acid (PLGA) nanoparticles as per 32 Factorial Design are presented. PLGA (X1) and PVA (Polyvinyl alcohol) solution (X2) as a stabilizing agent were used as independent variables where Particle size (PS) (Y1), Entrapment Efficiency (EE) (Y2) and % Drug Release at 12th h (REL)(Y3) were taken as dependant variables. Rifampicin nanoparticles were prepared by multiple emulsion solvent evaporation method. The results showed the method as reproducible, easy and efficient is the entrapment of drug as well as formation of spherical nanoparticles. Effect of polymer concentration was also evaluated with respect to their % drug entrapment efficiency. The in vitro release studies indicated the rifampicin-loaded PLGA nanoparticles provide sustained drug release over a period of 12h. The optimum batch was R3 which shown particle size 326 nm, 61.70 % EE and 57. 50% drug release at 12th h. Infrared spectroscopy analysis revealed that there was no known chemical interaction between drug and polymer. Hence, this investigation demonstrated the potential of the experimental design in understanding the effect of the formulation variables on the quality of rifampicin nanoparticles.

Menthol, Borneol, Camphor and WS-3 Eutectic Mixture

2012 ◽  
Vol 506 ◽  
pp. 355-358 ◽  
Author(s):  
S. Tuntarawongsa ◽  
T. Phaechamud
Keyword(s):  
Room Temperature ◽  
Chemical Interaction ◽  
Glass Plate ◽  
Eutectic Mixture ◽  
Contact Angle Measurement ◽  
Angle Measurement ◽  
Eutectic System ◽  
Newtonian Flow ◽  
Eutectic Systems ◽  
Unique Composition

Eutectic system is a mixture or solution which the ingredients solidify or liquefy simultaneously. A eutectic mixture is therefore that unique composition of two (or more) components that has the lower crystallization temperature or melting point. This aim of this study was to prepare and characterize the eutectic systems containing menthol, borneol, camphor and N-Ethyl-5-methyl-2-(1-methylethyl) cyclohexanecarboxamide (WS-3). Menthol is able to form liquid eutectic at room temperature with camphor in the ratio of 8:2, 7:3, 6:4 and 5:5 whereas menthol and borneol in the ratio of 8:2 and 7:3, menthol and WS-3 in the ratio of 6:4 and 1:1. The rheology behavior of all liquid eutectic systems was Newtonian flow which the surface tension was in the range of 28-29 mN/m. From contact angle measurement, all liquid eutectic systems were categorized as high wettability to the glass plate. The suitable liquid eutectic system for further application as liquid carrier for injectable active compounds was 1:1 menthol:camphor because of its lowest viscosity. IR spectra indicated that there was no chemical interaction of these two materials in the selected liquid eutectic mixture.

Influence of Formulation Variables and Processing Techniques on Drug Release from Carbopol-971 based Matrix Tablets of Cinnarizine and Nimodipine.

2010 ◽  
Vol 2 (1) ◽  
Author(s):  
Singh K. ◽  
Pandit K. ◽  
Mishra N.
Keyword(s):  
Drug Release ◽  
Release Rate ◽  
Polymer Concentration ◽  
Matrix Tablets ◽  
Wet Granulation ◽  
Weight Variation ◽  
Diffusion Controlled ◽  
The Matrix ◽  
Processing Techniques ◽  
Formulation Variables

The matrix tablets of cinnarizine and nimodipine were prepared with varying ratio of Carbopol- 971P and co-excipients of varying hydrophilicity (i.e. dicalcium phosphate and spray dried lactose) by direct compression and wet granulation using alcoholic mucilage. The prepared tablets were evaluated for weight variation, hardness and friability. The influence of concentration of the matrix forming material and co-excipients on the release rate of the drug was studied. The release rate of Cinnarizine (more soluble drug) from tablets followed diffusion controlled mechanism whereas for nimodipine (less soluble drug), the drug release followed case-II or super case- II transport mechanism based on Korsmeyer- Peppas equation. The results indicated that the drug release from matrix tablets was increases with increase in hydrophilicity of drug and co-excipients. The release of drug also increased with thermal treatment and decreasing polymer concentration.

Pharmaceutical Polymers - A Review

2019 ◽  
Vol 9 (01) ◽  
pp. 27-33
Author(s):  
Naveen Kumar ◽  
Sonia Pahuja ◽  
Ranjit Sharma
Keyword(s):  
Drug Release ◽  
Industrial Revolution ◽  
Pharmaceutical Formulations ◽  
Pharmaceutical Products ◽  
Water Soluble ◽  
Taste Masking ◽  
Natural Polymers ◽  
Pharmaceutical Dosage Forms ◽  
Pharmaceutical Applications ◽  
Pharmaceutical Industries

Humans have taken advantage of the adaptability of polymers for centuries in the form of resins, gums tars, and oils. However, it was not until the industrial revolution that the modern polymer industry began to develop. Polymers represent an important constituent of pharmaceutical dosage forms. Polymers have played vital roles in the formulation of pharmaceutical products. Polymers have been used as a major tool to manage the drug release rate from the formulations. Synthetic and natural-based polymers have found their way into the biomedical and pharmaceutical industries. Synthetic and Natural polymers can be produced with a broad range of strength, heat resistance, density, stiffness and even price. By constant research into the science and applications of polymers, they are playing an ever-increasing role in society. Diverse applications of polymers in the present pharmaceutical field are for controlled drug release. Based on solubility pharmaceutical polymers can be classified as water-soluble and water-insoluble. In general, the desirable polymer properties in pharmaceutical applications are film forming, adhesion, gelling, thickening, pH-dependent solubility and taste masking. General pharmaceutical applications of polymers in various pharmaceutical formulations are also discussed

Preparation and Evaluation of Gemifloxacin Mesylate Floating Matrix Tablets in Healthy Human Volunteers

2017 ◽  
Vol 10 (1) ◽  
pp. 3623-3630
Author(s):  
Bhikshapathi D. V. R. N. ◽  
Haarika B ◽  
Jyothi Sri S ◽  
K Abbulu
Keyword(s):  
Drug Release ◽  
Sodium Bicarbonate ◽  
Polymer Concentration ◽  
Hydroxypropyl Methylcellulose ◽  
Matrix Tablets ◽  
Physical Parameters ◽  
Drug Bioavailability ◽  
Floating Tablets

The purpose of present investigation was to develop floating matrix tablets of gemifloxacin mesylate, which after oral administration could prolong the gastric residence time, increase the drug bioavailability and diminish the side effects of irritating drugs. Tablets containing drug, various viscosity grades of hydroxypropyl methylcellulose such as HPMC K4M and HPMC K15M as matrix forming agent, Sodium bicarbonate as gas-forming agent and different additives were tested for their usefulness in formulating gastric floating tablets by direct compression method. The physical parameters, in vitro buoyancy, release characteristics and in vivo radiographic study were investigated in this study. The gemifloxacin mesylate floating tablets were prepared using HPMC K4M polymer giving more sustained drug release than the tablet containing HPMC K15M. All these formulations showed floating lag time of 30 to 47 sec and total floating time more than 12 h. The drug release was decreased when polymer concentration increases and gas generating agent decreases. Formulation that contains maximum concen-tration of both HPMC K15M and sodium bicarbonate (F9) showing sufficiently sustained with 99.2% of drug release at 12 h. The drug release from optimized formulation follows Higuchi model that indicates the diffusion controlled release. The best formulation (F9) was selected based on in vitro characteristics and used in vivo radiographic studies by incorporating barium sulphate as a radio-opaque agent and the tablet remained in the stomach for about 6 h.   

Formulation of Extended-Release Beads of Lamotrigine Based on Alginate and Cassia fistula Seed Gum by QbD Approach

2020 ◽  
Vol 17 (5) ◽  
pp. 422-437
Author(s):  
Dixita Jain ◽  
Akshay Sodani ◽  
Swapnanil Ray ◽  
Pranab Ghosh ◽  
Gouranga Nandi
Keyword(s):  
Drug Release ◽  
Factorial Design ◽  
Extended Release ◽  
Polymer Concentration ◽  
Green Manufacturing ◽  
Full Factorial Design ◽  
Cassia Fistula ◽  
Negative Environmental Impact ◽  
Seed Gum ◽  
Full Factorial

Aim: This study was focused on the formulation of the multi-unit extended-release peroral delivery device of lamotrigine for better management of epilepsy. Background: The single-unit extended-release peroral preparations often suffer from all-or-none effect. A significant number of multi-unit delivery systems have been reported as a solution to this problem. But most of them are found to be composed of synthetic, semi-synthetic or their combination having physiological toxicity as well as negative environmental impact. Therefore, fabrication and formulation of multi-unit extended-release peroral preparations with natural, non-toxic, biodegradable polymers employing green manufacturing processes are being appreciated worldwide. Objective: Lamotrigine-loaded extended-release multi-unit beads have been fabricated with the incorporation of a natural polysaccharide Cassia fistula seed gum in calcium-cross-linked alginate matrix employing a simple green process and 23 full factorial design. Methods: The total polymer concentration, polymer ratio and [CaCl2] were considered as independent formulation variables with two different levels of each for the experiment-design. The extended-release beads were then prepared by the ionotropic gelation method using calcium chloride as the crosslinkerions provider. The beads were then evaluated for drug encapsulation efficiency and drug release. ANOVA of all the dependent variables such as DEE, cumulative % drug release at 2h, 5h, 12h, rate constant and dissolution similarity factor (f2) was done by 23 full factorial design using Design-Expert software along with numerical optimization of the independent variables in order to meet USP-reference release profile. Results: The optimized batch showed excellent outcomes with DEE of 84.7 ± 2.7 (%), CPR2h of 8.41± 2.96 (%), CPR5h of 36.8± 4.7 (%), CPR12h of 87.3 ± 3.64 (%) and f2 of 65.9. Conclusion: This approach of the development of multi-unit oral devices utilizing natural polysaccharides might be inspiring towards the world-wide effort for green manufacturing of sustained-release drug products by the QbD route.

Preparation and Evaluation of Chitosan Loaded Naproxen Nanoparticles by Emulsion Interfacial Reaction Method

2019 ◽  
Vol 9 (2) ◽  
pp. 89-96
Author(s):  
Abbaraju Krishna Sailaja ◽  
Juveria Banu
Keyword(s):  
Drug Release ◽  
Interfacial Reaction ◽  
Polymer Concentration ◽  
Chitosan Nanoparticles ◽  
Particle Diameter ◽  
Entrapment Efficiency ◽  
Reaction Method ◽  
Release Data ◽  
Mean Particle Diameter

Aim: The aim of this investigation was to develop and characterize naproxen loaded chitosan nanoparticles by emulsion interfacial reaction method. Methodology: For emulsion interfacial reaction method chitosan was used as a polymer. In this method, eight formulations were prepared by varying drug to polymer concentration. Discussion: Out of eight formulations prepared using emulsion interfacial reaction method EI8 formulation was found to be the best formulation. The drug content was observed as 94.4%, entrapment efficiency and loading capacity were found to be 87.5% and 75%, respectively. The mean particle diameter was measured as 324.6nm and the Zeta potential value was found to be -42.4mv. In vitro drug release data showed 97.2% of drug release rate sustained up to 12hrs. Conclusion: The results clearly reveal that EI8 formulation having the highest amount of drug was considered as the best formulation because of its small mean particle diameter, good entrapment efficiency, and stability.

scholarly journals An Existence Theory for Gravity–Capillary Solitary Water Waves

Water Waves ◽  
2021 ◽  
Author(s):  
M. D. Groves
Keyword(s):  
Surface Tension ◽  
Water Waves ◽  
Applied Mathematics ◽  
Spatial Dynamics ◽  
Existence Theory ◽  
Water Wave Problem ◽  
Reduction Methods ◽  
Centre Manifold Reduction ◽  
Weak Surface ◽  
The One

AbstractIn the applied mathematics literature solitary gravity–capillary water waves are modelled by approximating the standard governing equations for water waves by a Korteweg-de Vries equation (for strong surface tension) or a nonlinear Schrödinger equation (for weak surface tension). These formal arguments have been justified by sophisticated techniques such as spatial dynamics and centre-manifold reduction methods on the one hand and variational methods on the other. This article presents a complete, self-contained account of an alternative, simpler approach in which one works directly with the Zakharov–Craig–Sulem formulation of the water-wave problem and uses only rudimentary fixed-point arguments and Fourier analysis.

PREPARATION, EVALUATION AND OPTIMIZATION OF MUCOADHESIVE MINI TABLETS OF TELMISARTAN BY USING SINGLE UNIT ENCAPSULATION SYSTEM

INDIAN DRUGS ◽  
2019 ◽  
pp. 64-67
Author(s):  
Indrajeet S. Patil ◽  
Omkar A. Patil ◽  
Rohankumar R. Chavan ◽  
Dheeraj S. Randive ◽  
Mangesh A. Bhutkar ◽  
...  
Keyword(s):  
Drug Release ◽  
Single Unit ◽  
Chemical Interaction ◽  
Extended Period ◽  
Controlled Drug Release ◽  
Wet Granulation ◽  
Dissolution Study ◽  
Capsule Shell ◽  
Physical And Chemical

The objective of the present study was to develop and optimize capsule filled oral mucoadhesive minitablets of telmisartan. Wet granulation method was employed for the development of minitablets. All the formulations (F1- F13) exhibited more than 21% drug release at 4h and at the end of 12h it showed drug release more than 90%. During the dissolution study it was observed that the capsule shell in which the minitablets were filled got completely dissolved in the first 5 min. FTIR and UV study showed absence of any significant physical and chemical interaction between drug and polymers. Formulation F 10 was found to possess higher drug release at 4h and 12 h. Combination of HPMC and Carbopol was found to be suitable for formulation of mucoadhesive minitablets, showed promising mucoadhesive strength and exhibited controlled drug release over an extended period of time.

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