Resveratrol-loaded calcium-pectinate beads: Effects of formulation parameters on drug release and bead characteristics

2010 ◽  
Vol 99 (2) ◽  
pp. 840-860 ◽  
Author(s):  
Surajit Das ◽  
Ka-Yun Ng
Keyword(s):  
Drug Release ◽  
Calcium Pectinate ◽  
Formulation Parameters

Pectin-Chitosan Multilayer Coated Microbeads of Diclofenac Sodium Prepared by Layer-by-Layer Technique

2014 ◽  
Vol 1060 ◽  
pp. 45-49
Author(s):  
Kamonrak Cheewatanakornkool ◽  
Pornsak Sriamornsak
Keyword(s):  
Controlled Release ◽  
Drug Release ◽  
Diclofenac Sodium ◽  
Gastric Fluid ◽  
Layer By Layer ◽  
Release Behavior ◽  
Freeze Dried ◽  
Layer Technique ◽  
Calcium Pectinate ◽  
Layer By Layer Technique

The main objective of this study was to fabricate biopolymer-based microbeads, providing enteric properties and controlled release of diclofenac sodium, using layer-by-layer technique. The calcium pectinate microbeads have been designed and coated with chitosan and pectin multilayers. Drug release was performed in simulate gastric fluid (pH 1.2) for 2 hours, followed by pH 6.8 buffer for 8 hours. The effects of chitosan concentration, number of layer and drying technique on drug release were investigated. The results showed that the calcium pectinate microbeads could be simply prepared by ionotropic gelation and then coated with chitosan and pectin solutions using layer-by-layer procedure. The diameter of the microbeads ranged from 800 to 1000 μm for air-dried samples and from 1 to 2 mm for freeze-dried samples. The freeze-dried microbeads had a rough surface and many pores inside, as observed by SEM. The microbeads coated with 4% chitosan/4% pectin revealed a slower drug release than those coated with 1% chitosan/4% pectin and demonstrated a controlled release pattern. Moreover, different drying techniques and numbers of layer also influenced drug release behavior of the prepared microbeads.

DEVELOPMENT AND EVALUATION OF MODIFIED RELEASE MATRIX TABLETS OF MILNACIPRAN HCL USING MELT GRANULATION TECHNIQUE

INDIAN DRUGS ◽  
2018 ◽  
Vol 55 (02) ◽  
pp. 68-71
Author(s):  
N. C Ratnakara ◽  
◽  
M. C. Gohel
Keyword(s):  
Drug Release ◽  
Matrix Tablets ◽  
Matrix Tablet ◽  
Modified Release ◽  
Independent Variables ◽  
Dependent Variables ◽  
Formulation Parameters ◽  
Predicted Values ◽  
Melt Granulation

The objective of the present study was to identify critical formulation parameters affecting the drug release from modified release wax matrix tablet of milnacipran hydrochloride employing the concept of design of experiments.The optimized amount of Compritol 888 ATO(intragranular) (X1), lactose (X2) and Compritol 888ATO (extragranular)(X3) were determined employing simplex latticedesign. The tablets were prepared using melt granulation technique. The in vitro drug release study was carried out in an acidic medium (pH 1.2) for 2 h and thereafter the dissolution study was conducted in phosphate buffer (pH 6.8).The selected dependent variables were the cumulative percentage of milnacipran hydrochloride dissolved at 1 (Y1), 8 (Y8), 16 (Y16) and 24 h (Y24). Mathematical models, correlating the independent variables with dependent variables were evolved. Optimization was performed for the three independent variables using the stated target ranges; Y1≤20%; Y8=45±5%; Y16=72±5%; Y24=100%. The optimized amounts of Compritol ATO888 (intragranular)(X1), lactose (X2) and Compritol 888ATO (extragranular)(X3), were found to be 60, 55 and 30 mg, respectively.The optimized formulation showed a release profile that was close to the predicted values. The drug was released by anomalous diffusion from the optimized formulation. Compritol 888ATO (intragranular) (X1), lactose (X2) and Compritol 888ATO(extragranular) (X3) were identified as critical variables.

scholarly journals Effect of Drug Loading Method on Drug Content and Drug Release from Calcium Pectinate Gel Beads

2010 ◽  
Vol 11 (3) ◽  
pp. 1315-1319 ◽  
Author(s):  
Pornsak Sriamornsak ◽  
Jurairat Nunthanid ◽  
Kamonrak Cheewatanakornkool ◽  
Somkamol Manchun
Keyword(s):  
Drug Release ◽  
Drug Loading ◽  
Drug Content ◽  
Loading Method ◽  
Gel Beads ◽  
Calcium Pectinate

scholarly journals Effect of formulation parameters on the drug release and floating properties of gastric floating two-layer tablets with acetylsalicylic acid

2011 ◽  
Vol 61 (3) ◽  
pp. 303-312 ◽  
Author(s):  
Canan Hasçiçek ◽  
Günseli Yüksel-Tilkan ◽  
Berna Türkmen ◽  
Nurten Özdemir
Keyword(s):  
Drug Release ◽  
Acetylsalicylic Acid ◽  
Drug Loading ◽  
Hydroxypropyl Methylcellulose ◽  
High Viscosity ◽  
Compression Technique ◽  
Gastric Residence Time ◽  
Low Viscosity ◽  
Formulation Parameters ◽  
Floating Layer

Effect of formulation parameters on the drug release and floating properties of gastric floating two-layer tablets with acetylsalicylic acid Floating dosage forms of acetylsalicylic acid, used for its antithrombotic effect, were developed to prolong gastric residence time and increase bioavailability. In the two-layer tablet formulation, hydroxypropyl methylcellulose (HPMC) of high viscosity and an effervescent mixture of citric acid and sodium bicarbonate formed the floating layer. The release layer contained the drug, direct tableting agent and different types of matrix-forming polymers such as HPMC of low viscosity, sodium carboxymethylcellulose and chitosan. Tablets were prepared using a direct compression technique. The effect of formulation variables on physicochemical and floating properties and the drug release from tablets were investigated. Floating ability was dependent on the amount of effervescent agent and gel-forming polymer of the floating layer. Drug release was prolonged to 8 hours by changing the type and viscosity of the matrix-forming polymer in the drug-loading layer and all formulations showed a diffusion release mechanisms.

Pulsatile Drug Delivery Systems: An Overview

2009 ◽  
Vol 2 (3) ◽  
pp. 605-614
Author(s):  
Ramesh D. Parmar ◽  
Rajesh K. Parikh ◽  
G. Vidyasagar ◽  
Dhaval V. Patel ◽  
Chirag J. Patel ◽  
...  
Keyword(s):  
Drug Delivery ◽  
Drug Release ◽  
Drug Delivery Systems ◽  
Delivery Systems ◽  
The Body ◽  
Night Time ◽  
Technological Developments ◽  
Pulsatile Drug Delivery ◽  
Formulation Parameters ◽  
The Right

Pulsatile  Drug  Delivery  Systems  are  gaining  a  lot  of  interest  as  they  deliver  the  drug  at  the  right  place  at  the  right  time  and  in  the  right  amount,  thus  providing  spatial  and  temporal  delivery  and  increasing  patient  compliance.  These  systems  are  designed  according  to  the  circadian  rhythm  of  the  body.  The  principle  rationale  for  the  use  of  pulsatile  release  of  the  drugs is where  a  constant  drug  release  is  not  desired.  A  pulse  has  to  be  designed  in  such  a  way  that  a  complete  and  rapid  drug  release  is  achieved  after  the  lag  time.  Various  systems  like  capsular  systems,  osmotic  systems,  single-  and  multiple-unit  systems  based  on  the  use  of  soluble  or  erodible  polymer  coating  and  use  of  rupturable  membranes  have  been  dealt  with  in  the  article.  It  summarizes  the  latest  technological  developments,  formulation  parameters,  and  release  profiles  of  these  systems.  These  systems  are  beneficial  for  the  drugs  having  chronopharmacological  behavior  where  night  time  dosing  is  required,  such  as  anti-arhythmic  and  anti-asthmatic.

Methotrexate Bearing Calcium Pectinate Microspheres: A Platform to Achieve Colon-Specific Drug Release

2008 ◽  
Vol 5 (3) ◽  
pp. 215-219 ◽  
Author(s):  
M. Chaurasia ◽  
M. Chourasia ◽  
Nitin Jain ◽  
A. Jain ◽  
V. Soni ◽  
...  
Keyword(s):  
Drug Release ◽  
Specific Drug ◽  
Calcium Pectinate

Lipid-Based Implants: Impact of Formulation Parameters

2014 ◽  
Vol 1060 ◽  
pp. 87-90
Author(s):  
Marisa Nicolai ◽  
Vanessa Amaral ◽  
Cátia Antunes ◽  
Duangratana Shuwisitkul ◽  
Joana Portugal Mota
Keyword(s):  
Controlled Release ◽  
Drug Release ◽  
Release Rate ◽  
Release Rates ◽  
Drug Release Rate ◽  
Blend Ratio ◽  
Drug Type ◽  
Formulation Parameters ◽  
Blend Ratios ◽  
Aqueous Solubilities

Lipid implants have been attracting attention in recent years. However, to better understand these systems, more fundamental studies are required. The objective of this work was to evaluate the effect of some formulation parameters, namely lipid and drug type, implant shape/surface area and lipid blend ratio, on drug release rate. The developed implants were cylindrical or spherical in shape with an even surface. Caffeine release from glycerol-trimyristate implant was very fast when compared with glycerol-tristerate matrix. The latter allowed a 4 month controlled release in contrast with glycerol-trimyristate matrix (~ 5 days). Caffeine and theophylline presented similar release rates, despite their different aqueous solubilities. In addition, different lipid blend ratios provided different release profiles for caffeine.

scholarly journals Mechanical characterization of calcium pectinate hydrogel for controlled drug delivery

2003 ◽  
Vol 57 (12) ◽  
pp. 611-616 ◽  
Author(s):  
Jin Chung ◽  
Zhang Zhibing
Keyword(s):  
Mechanical Properties ◽  
Drug Release ◽  
Oral Delivery ◽  
Drug Carrier ◽  
Release Profile ◽  
Water Soluble ◽  
Drug Release Profile ◽  
Force Relaxation ◽  
Calcium Pectinate ◽  
Model Drug

Calcium pectinate beads, a paniculate hydrogel system, is an attractive drug carrier for oral delivery. In this study, a poorly water-soluble model drug indomethacin was incorporated into calcium pectinate beads made of different pectin concentrations, which were produced by an extrusion method. The effect of pectin concentration on bead size, circularity, swelling behavior, and mechanical properties, as well as in vitro drug release profile was investigated. The mechanical properties of calcium pectinate beads were determined by a micromanipulation technique. The drug release profile was measured using a standard British Pharmacopoeia method. It was found that the beads made of higher pectin concentration in general had a less permeable matrix structure and greater mechanical rigidity, although they swelled more after hydration. However, such an effect was not significant when the pectin concentration was increased to above 8%. Micromanipulation measurements showed that there was significant relaxation of the force being imposed on single hydrated beads when they were held, but this phenomenon did not occur on dry beads, which means that the force relaxation was dominated by liquid loss from the beads. The rate of the force relaxation was determined, and has been related to the release rate of the model drug entrapped in the calcium pectinate beads.

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