The Potential Of Tamarind Seed Polysaccharide Biology Essay

M.U. Mishra33 et al.

, undertaken to measure the potency of Tamarind seed polyose to move as a biodegradable bearer for colon specific drug bringing. The matrix tablets were prepared by wet granulation technique incorporating different concentrations ( 30 % w/w to 70 % w/w ) of TSP utilizing Ibuprofen as a exemplary drug. The consequences of in vitro drug release survey indicate that the matrix tablets prepared by utilizing TSP are able to transport most of the drug to the colon and curtail the release in upper GIT.

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Rishabha Malviya34 et Al ( 2010 ) was made to explicate sustained release matrix tablets of Diclofenac Na utilizing gum acacia and tamarind gum as release qualifier. Six batches of sustained release matrix tablets of Diclofenac Na were prepared by utilizing different drug: polymer ratios viz. 1:1, 1:1.5, 1:2, 1:2.5,1:3, and 1:3.

5 for both gum acacia and Tamarindus indica gum. Consequences showed that the drug release from matrix tablets prepared by utilizing natural polymers can be sustained for more than 12 hour and the drug release vary with concentration of polymer in matrix tablets.Srivastava Pranati35 et Al ( 2010 ) made to increase curative effectivity, cut down dose frequence and so betterment in patient conformity, by developing sustained release matrix tablets utilizing Tamarindus indica gum and pectin as release qualifier. Six batches of sustained release matrix tablets of Diclofenac Na were prepared by utilizing different drug: polymer ratios viz.

1:1, 1:1.5, 1:2, 1:2.5, 1:3, 1:3.5 for Tamarindus indica gum and pectin. A better sustained release was obtained with the matrix tablet of Tamarindus indica gum. It is cleared that the drug release from matrix tablets prepared by utilizing tamarind gum can be sustained for more than 12 hour and release of drug vary with concentration of polymers in matrix tablets.Pratik Shah36 et Al ( 2010 ) research was developed and measure a matrix system for Chronotherapeutic bringing of NSAID ( Non-steroidal anti-inflammatory drug ) incorporating Natural polyose in Rheumatoid Arthritis.

The natural polyoses, Guar gum, were used as a bearer for drug bringing along with three different polymeric binders to optimise the proper preparation for Chronotherapeutic drug bringing. Different bathes of matrix tablet Of Diclofenac Sodium- Guar gum were prepared utilizing wet granulation method. The release profile of Diclofenac Sodium from the matrix tablets is dependent upon the gelling belongings of Guar gum and debasement of Guar gum by colonic bacteriums. It is concluded from the present probe that Guar gum incorporating matrix tablets are assuring controlled release systems for colon-targeted bringing of Diclofenac Na.V.V.

Kale37 et Al ( 2010 ) investigated the significance of factors such as drug solubility, proportion of polymers and other linear on drug release from cluster bean gum based matrix system. Pseudoephedrine HCl, Metformin, Tetracycline and Diclofenac Na with solubilities & gt ; 50 % & lt ; _ % & lt ; _10 % ,0.1 % severally were used as drug theoretical accounts. As the cluster bean gum content was increased, drug release rate was decreased. When the cluster bean gum and drug proportion was changeless, alteration in the rate of drug release was observed with the alteration in the drug solubility.Rishabha Malviya38 et Al ( 2010 ) effort was made to increase curative effectivity, decrease in dosing frequence and therefore bettering patient conformity, by developing sustained release matrix tablets of Diclofenac Na utilizing guar gum as release qualifier. Six batches of sustained release matrix tablets of Diclofenac Na was prepared by utilizing different drug: polymer ratios viz.

1:1, 1:1.5, 1:2, 1:2.5, 1:3, 1:3.5 for cluster bean gum. Result show that as the concentration of gum additions, swelling index besides increased proportionately.

It is clear through the disintegration surveies that the release profile of Diclofenac Na from matrix tablets prepared utilizing cluster bean gum was retarded about 24h.Gurpreet Kaur39 et Al ( 2010 ) The present survey was designed to explicate colon release tablets of fluticasone by using cross linked chitosan ( CH ) and carboxymethyl cluster bean gum ( CMG ) inter polymer composites ( IPC ) . Matrix tablets were prepared by wet granulation method utilizing IPC as binder and surfacing agent.The uncoated and coated tablets were tested for their suitableness as colon specific drug bringing system by in vitro disintegration surveies. The coated tablets were evaluated for their pharmacodynamic public presentation after unwritten disposal to TNBS induced ulcerative inflammatory bowel disease rats. Histopathology of the rat colon after unwritten disposal of these IPC movie coated tablets revealed significantly greater ( P & lt ; 0.05 ) decrease in TNBS-induced ulcerative inflammatory bowel disease The survey confirmed that selective bringing of fluticasone to the colon can be achieved utilizing cross-linked CH and CMG polyoses.Hindustan Abdul Ahad40 et Al ( 2010 ) probe was to develop matrix tablets of Aceclofenac with Prosophis juliflora gum and to analyze its functionality as a matrix forming agent for one time day-to-day sustained release tablet preparations.

Physicochemical belongingss of dried powdered Prosophis juliflora gum were studied. Assorted preparations of Aceclofenac Prosophis juliflora gum were prepared.The disintegration survey proved that the dried Prosophis juliflora gum can be used as a matrix organizing stuff for doing one time day-to-day Sustained release matrix tablets.Santanu Ghosh41 et Al ( 2010 ) was to develop matrix tablets for unwritten controlled release of aceclofenac. Matrix tablets of aceclofenac, utilizing assorted viscousness of hydrophilic polymer HPMC in two different proportions, hydrophobic polymer ethyl cellulose and Guar gum were prepared by wet granulation method and subjected to in vitro drug release surveies. The drug release from all HPMC matrix tablets followed assorted release dynamicss, preparation no -F7 followed higuchi dynamicss. Furthermore, the consequences of the in vitro surveies in pH 7.5 phosphate buffer medium showed that F7 tablets provided controlled release comparable with market sustained release preparation ( Aeroff-SR tablets ) .

F7 tablets showed no alteration in physical visual aspect, drug content, or in disintegration form after storage at 40A°C with 75 % RH for 6 months. Based on the consequences of the in vitro surveies, it was concluded that the HPMC matrix tablets provided unwritten controlled release of aceclofenac.Santanu Ghosh and Barik42 et Al ( 2010 ) was to develop matrix tablets for unwritten controlled release of aceclofenac utilizing ethyl cellulose, cluster bean gum, and assorted classs of cellulose polymers.

The release profile of one of the formulated aceclofenac tablets, which contained hydroxypropyl methyl cellulose, was statistically similar to that of the commercial aceclofenac trade name in all the disintegration media. The consequence indicate that it is executable to accomplish a stable one time day-to-day sustained release aceclofenac tablet preparation by utilizing HPMC k4M of 4000cps viscousness class as matrix stuff.Suresh V Kulkarni43 et Al ( 2010 ) probe an effort was made to cut down the frequence of dose disposal and to better the patient conformity by developing controlled release ( CR ) matrix tablet of Stavudine utilizing of course happening ( Guar gum and Xanthun gums ) and Man-made Polymers ( HPMC and Ethyl cellulose ) . Six batches of CR matrix tablets of Stavudine were developed by utilizing wet granulation technique.

Tablets were evaluated for weight fluctuation, hardness, crumbliness and In vitro disintegration surveies. All preparation showed conformity with pharmacopoeial criterions. Among the six preparations, F3 showed controlled release of drug for 12 hours with 91.

65 % drug release. The release information was fitted to assorted mathematical theoretical accounts such as, Higuchi, Korsmeyer-Peppas, First-order, and Zero-order to measure the dynamicss and mechanism of the drug release was found to be diffusion coupled witherosion.Amit K Nagariya44 et Al ( 2010 ) made in the research and development of rate-controlled unwritten drug bringing systems by get the better ofing physiological hardships, such as short gastric abode times ( GRT ) and unpredictable gastric emptying times ( GET ) .

Several approaches a recurrently utilized in the protraction of the GRT, including drifting drug bringing systems ( FDDS ) , Gastro retentive drifting drug bringing systems ( GFDDS ) are the systems which are retained in the tummy for a longer period of clip and thereby better the bioavailability of drugs. Natural polymer shave a figure of advantages like Biocompatibility, Natural in beginning, biodegradable to normal organic structure components, safe and non-toxic. Natural gums are among the most popular hydrophilic polymers because of their cost-effectiveness and regulative credence.

In this paper we have tried to give a brief over position to the potency of natural polymer in the development of gastro recollective drifting drug bringing system.Dr.Umesh.

D.Shivhare45 et Al ( 2009 ) was to develop “ one time day-to-day ” sustained release tablets of aceclofenac by wet granulation utilizing carboxypolymethylene polymer. The drug excipient mixtures were subjected to preformulation surveies while the tablets were subjected to physicochemical surveies, in vitro drug release, stableness surveies andvalidation surveies.

The physicochemical belongingss of tablets were found within the bounds. Formulation F2 & A ; F9containing Carbopol 971P and Carbopol 974P were found to let go of the drug in sustained mode up to 24 hr were stable under accelerated conditions of temperature for 6 months since there were no important alterations in drug content and physical parametric quantities.Raghavendra Rao N. G46 et Al ( 2009 ) was to develop sustained release matrix tablets of H2O soluble Tramadol hydrochloride utilizing different polymers viz. Hydroxy propyl methyl cellulose ( HPMC ) and natural gums like Karaya gum ( KG ) and Carrageenan ( CG ) .

Changing ratios of drug and polymer like 1:1 and 1:2 were selected for the survey. After repairing the ratio of drug and polymer for control the release of drug up to coveted clip, the release rates were modulated by combination of two different rates commanding stuff and ternary mixture of three different rate commanding stuff. After rating of physical belongingss of tablet, the in vitro release survey was performed in 0.1N HCl pH 1.2 for 2 hour and in phosphate buffer pH 6.

8 up to 12 hour. The consequence of polymer concentration and polymer blend concentration were studied. Different ratios like 80:20, 60:40, 50:50, 40:60 and 20:80 were taken. Dissolution information was analyzed by Korsmeyer- Peppas power jurisprudence look and modified power jurisprudence look.

It was observed that matrix tablets contained polymer blend of HPMC/CG were successfully sustained the release of drug upto 12 hour. Among all the preparations, preparation F16 which contains 20 % HPMC K15M and 80 % of CG let go of the drug which follow Zero order dynamicss via, swelling, diffusion and eroding and the release profile of preparation F16 was comparable with the marketed merchandise. Stability surveies ( 40A±2°C/75A±5 % RH ) for 3 months indicated that Tramadol hydrochloride was stable in the matrix tablets. The DSC and FTIR survey revealed that there was no chemical interaction between drug and excipients.Bhavin Patel47 et Al ( 2009 ) were fabricated the buccal mucoadhesive tablets of Procardia with aim of avoiding first base on balls metamorphosis and protracting continuance of action.

The mucoadhesive polymers used in preparations were carbopol ( cp934 ) , hydroxyl propyl methyl cellulose ( HPMC K4M ) , carboxy methyl cellulose ( CMC ) , and tamarind seed polyose ( TSP ) .These preparations were characterized for physiochemical parametric quantities, in vitro keeping clip, in vitro bioadhesive strength, per centum hydration and drug release. The modified in vitro assembly was used to mensurate the bioadhesive strength of tablets with fresh caprine animal buccal mucous membrane as a theoretical account tissue. The best mucoadhesive public presentation and in vitro drug release profile were exhibited by the tablet containg carbopol and TSP in the ratio of 1:1. This preparation was more comfy to the user due to less eroding, faster hydration rate, and optimal pH of environing medium.UK Patil48 et Al ( 2008 ) were fabricated utilizing pectin, guar gum and xanthan gum. The tablets were evaluated for physical feature like hardness, weight fluctuation, fraibilty, and drug content.

In-vitro release of drug was performed in PBS pH 7.2 for 15 hours. All the physical characters of the fancied tablet were within acceptablebounds. The tablet with guar gum exhibited greater swelling index than those with pectin and xanthan gum. A better controlled drug release ( 80.

74 % ) was obtained with the matrix tablet ( G4 ) made-up of the cluster bean gum than with the pectin and xanthan gum. It is cleared through the disintegration profile of Lasix from matrix tablets prepared utilizing different natural polymers were retarded about 15 hour.Reasonably M. Sankalia49 et Al ( 2008 ) was to analyze a degree A in vitro-in vivo correlativity ( IVIVC ) for glipizide hydrophilic sustained-release matrices, with an acceptable internal predictability, in the presence of a scope of formulation/manufacturing alterations. The consequence of polymeric blends of ethyl cellulose, microcrystalline cellulose, hydroxy propyl methylcellulose, xanthan gum, cluster bean gum, Starch 1500, and lactose on in vitro release profiles was studied and fitted to assorted release dynamicss theoretical accounts. Water uptake dynamicss with scanning electronmicroscopy ( SEM ) was carried out to back up the drug release mechanism.

An IVIVC was established by comparing the pharmacokinetic parametric quantities of optimized ( M-24 ) and marketed ( Glytop-2.5 SR ) preparations after individual unwritten dosage surveies on white albino coneies. The matrix M-19 ( xanthan: MCC PH301 at 70:40 ) and M-24 ( xanthan: HPMC K4M: Starch1500 at 70:25:15 ) showed the Glucotrol release within the preset restraints at all clip points with Korsmeyer-Peppas ‘ and zero-order release mechanism, severally. Kopcha theoretical account revealed that the xanthan gum is the major excipient responsible for the diffusional release profile and was farther supported by SEM and swelling surveies.

A important degree A IVIVC with acceptable bounds of anticipation mistakes ( below 15 % ) enables the anticipation of in vivo public presentation from their in vitro release profile. It was concluded that proper choice of rate commanding polymers with release rate qualifier excipients will find overall release profile, continuance and mechanism from straight compressed matrices.Jaleh Varshosaz50 et Al ( 2006 ) was to develop matrix sustained release tablets of extremely water-soluble tramadol HCl utilizing natural gums ( xanthan [ X gum ] and guar [ G gum ] ) as costeffective, nontoxic, easy available, and suited hydrophilic matrix systems compared with the extensively investigated hydrophilic matrices ( Internet Explorer, hydroxypropyl methylcellulose [ HPMC ] / carboxymethyl cellulose [ CMC ] with regard to in vitro drug release rate ) and hydration rate of the polymers. Matrix tablets of tramadol ( dose 100 milligram ) were produced by direct compaction method. Different ratios of 100:0, 80:20,60:40, 20:80, 0:100 of G gum ( or X ) : HPMC, X gum: G gum, and ternary mixture of these polymers ( G gum, X gum, HPMC ) were applied. After rating of physical features of tablets, the disintegration trial was performed in the phosphate buffer media ( pH 7.4 ) up to 8 hours.

Tablets with lone Ten had the highest average disintegration clip ( MDT ) , the least disintegration efficiency ( DE8 % ) , and released the drug following a zero-order theoretical account via swelling, diffusion, and eroding mechanisms. Guar gum entirely could non expeditiously command the drug release, while X and all combinations of natural gums with HPMC could retard tramadol HCl release. However, harmonizing to the similarity factor ( f2 ) , pure HPMC and H8G2 were the most similar preparations to Topalgic-LP as the mention criterion.

Saleh Al ( 2005 ) was to develop guar gum matrix tablets for unwritten controlled release of water-soluble Cardizem hydrochloride. Matrix tablets of Cardizem hydrochloride, utilizing assorted viscousness classs of cluster bean gum in 2 proportions, were prepared by wet granulation method and subjected to in vitro drug release surveies Based on the consequences of in vitro and in vivo surveies it was concluded that that cluster bean gum matrix tablets provided unwritten controlled release of water-soluble Cardizem hydrochloride.Tejraj M. Aminabhavi52 et Al ( 2004 ) was prepared by taking three different ratios of cluster bean gum to acrylamide ( 1:2, 1:3.5 and 1:5 ) .

Amide groups of these grafted copolymers were converted into carboxylic functional groups. Tablets were prepared by integrating an antihypertensive drug viz. , diltiazem hydrochloride.

In-vitro drug release was carried out in fake gastric and enteric conditions. Effect of drug burden on release dynamicss was evaluated. Release continued up to8 and 12 H, severally, for pAAm-g-GG and hydrolyzed pAAm-g-GG copolymers. Nature of drug conveyance through the polymer matrices was studied by comparing with Higuchi, Hixson-Crowell and Kopcha equations.

Drug release was found to be dissolution-controlled in instance of unhydrolyzed copolymer. With hydrolyzed copolymers, drug release was swelling controlled ab initio ( i.e. , in 0.

1 N HCl ) , but at subsequently phase, it became dissolution-controlled in pH 7.4. Hydrolyzed pAAm-g-GG matrices are pH sensitive and can be used for enteric drug bringing.Y.S.R. Krishnaiah53 et Al ( 2004 ) was to transport out pharmacokinetic rating of unwritten controlled release preparation ( guar gum-based three bed matrix tablets ) incorporating extremely soluble Lopressor tartrate as a exemplary drug.

The consequences of the survey indicated that guar gum three-layer matrix tablets were able to supply unwritten controlled bringing of extremely water-soluble drug such as metoprolol tartrate in worlds.Alor R. Ray54 et Al ( 2003 ) studied the function of modulating factors such as drug to polymer ratio, drug burden, atom size, and compression force per unit area ant sum of lubricator on release Caffeine from Tamarindus indica seed polyose, which is for hydrophilic matrix for drug bringing system. The undermentioned observation on release rate were made utilizing Korsmeyer-Peppas ‘s and Higuchi ‘s equations i ) the compression force per unit area had no important consequence on release.

two ) the consequence of atom size polyose on release was undistinguished except in the scope of 250-150 micrometers. three ) the addition in polymer content showed lessenings in both rate of release and disintegration. Iv ) the addition in drug burden showed the rate of release and disintegration decreased. V ) the presence of lubricator up to 2 % had no consequence on the rate of release. The mechanism of release was found to be anomalous ( n & gt ; 0.

5 ) in all the instances.Y.S.R. Krishnaiah55 et Al ( 2002 ) designed unwritten controlled drug bringing systems for extremely water-soluble drugs utilizing cluster bean gum as a bearer in the signifier of a three-layer matrix tablet.

The consequences indicated that cluster bean gum, in the signifier of three-layer matrix tablets, is a possible bearer in the design of unwritten controlled drug bringing systems for extremely water-soluble drugs such as metoprolol tartrate.


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