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

Abstract:

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.

journal_name

Curr Drug Deliv

journal_title

Current drug delivery

authors

Jain D,Sodani A,Ray S,Ghosh P,Nandi G

doi

10.2174/1567201817666200317124022

subject

Has Abstract

pub_date

2020-01-01 00:00:00

pages

422-437

issue

5

eissn

1567-2018

issn

1875-5704

pii

CDD-EPUB-105310

journal_volume

17

pub_type

杂志文章
  • Influence of drug incorporation, temperature and storage time on the pH, textural and rheological properties of different poloxamer hydrogels.

    abstract::In recent years, Poloxamers had attracted a particular interest in the design of dermal and transdermal delivery systems in order to improve or retard drug permeation through the skin. In the present study, the influence of different parameters, such as, temperature, storage time, type of polymer (Lutrol(®) F-127 and ...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:10.2174/15672018113109990056

    authors: Almeida H,Amaral MH,Lobão P,Lobo JM

    更新日期:2013-12-01 00:00:00

  • Studies with emulsion containing trans-resveratrol: in vitro release profile and ex vivo human skin permeation.

    abstract::Resveratrol is a phenolic compound that has been widely studied in the last years because of its extensive pharmacological properties. It also has physicochemical properties that are adequate for diffusion through the human skin. An analytical method by high performance liquid chromatography was developed and validate...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:10.2174/1567201812666150130161736

    authors: de Almeida PA,Alves MC,Polonini HC,Calixto SL,Braga Gomes TB,Barros Lataliza AA,da Silveira Ramos CD,Barbosa Raposo NR,de Oliveira Ferreira A,Fernandes Brandão A

    更新日期:2015-01-01 00:00:00

  • A Microstructural Study of the O/W Primary Emulsion on the Formation of Oil-in-Water-in-Oil Multiple Emulsion.

    abstract:AIM:This study aimed to investigate the influence of the preparation process and composition on the microstructure of the O/W primary emulsions and the corresponding impact on the formation of oil-in-water-in-oil (O/W/O) multiple emulsions. OBJECTIVES:Multiple emulsions were prepared by a two-step emulsification metho...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:10.2174/1567201818666210101114517

    authors: Zhang Q,Qin Y,Duan G,Ou W,Wang Y,Zhang W

    更新日期:2020-12-31 00:00:00

  • Anti-lung Cancer and Anti-angiogenic Activities of New Designed Boronated Phenylalanine Metal Complexes.

    abstract:BACKGROUND:Drug design and discovery studies still remain of great importance in the search for more convenient chemotherapeutic to avoid the drug resistance, systemic toxicity or the longterm side effects. OBJECTIVE:A series of mononuclear gold (III) and platinum (II) complexes based on 4-dihydroxyboryl- DL-phenylala...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:10.2174/1567201815666180727145724

    authors: Varol M,Koparal AT,Benkli K,Bostancioglu RB

    更新日期:2018-01-01 00:00:00

  • A gastroretentive drug delivery system of lisinopril imbibed on isabgol-husk.

    abstract::The gastroretentive drug delivery system is site-specific and allows the drug to remain in the stomach for a prolonged period of time so that it can be released in a controlled manner in gastrointestinal tract. The present study was carried out to develop a gastroretentive drug delivery system using isabgol as an exci...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:10.2174/15672018113106660065

    authors: Semwal R,Semwal RB,Semwal DK

    更新日期:2014-01-01 00:00:00

  • ADMET-Multi-Output Cheminformatics Models for Drug Delivery, Interactomics, and Nanotoxicology.

    abstract::ADMET Chemoinformatics multi-output models are useful for a parallel prediction of multiple experimental parameters related the absorption (A), distribution (D), metabolism (M), excretion (E), and toxicity (T) process of drugs, pollutants, and NPs with a single QSPR model. Here we present one state-of-art review about...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:

    authors: González-Díaz H

    更新日期:2016-04-19 00:00:00

  • Improved In vivo Effect of Chrysin as an Absorption Enhancer Via the Preparation of Ternary Solid Dispersion with Brij®L4 and Aminoclay.

    abstract:BACKGROUND:Chrysin is a strong inhibitor of breast cancer resistance protein (BCRP) but it is practically insoluble in water. Effective solubilization of chrysin is critical for its pharmaceutical application as an absorption enhancer via inhibition of BCRP-mediated drug efflux. OBJECTIVE:This study aimed to develop a...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:10.2174/1567201815666180924151458

    authors: Lee SH,Lee YS,Song JG,Han HK

    更新日期:2019-01-01 00:00:00

  • Investigation of in vitro iontophoresis facilitated transdermal delivery of glycine.

    abstract::The research presented in this paper discusses the potential of iontophoresis facilitated transdermal delivery of glycine. Iontophoresis has been widely investigated as a noninvasive transdermal drug delivery system. Iontophoresis is the use of a low electric current to carry ionized as well as unionized drug molecule...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:10.2174/156720109787846207

    authors: Dasgupta R,Banthia AK,Tibarewala DN

    更新日期:2009-04-01 00:00:00

  • Development of Atovaquone Nanosuspension: Quality by Design Approach.

    abstract:OBJECTIVE:The present study reports the use of MicrofluidizerTM technology to form a stable nanosuspension of atovaquone (ATQ) using quality by design (QbD) approach. METHODS:The patient-centric quality target product profile and critical quality attributes (CQAs) were identified. A Box-Behnken design was employed for...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:10.2174/1567201817666191227095019

    authors: Kakade P,Gite S,Patravale V

    更新日期:2020-01-01 00:00:00

  • In vitro Evaluation of Genipin-crosslinked Na-alginate/Chitosan Hydrogel Films for Delivery of Metformin: Effect of Chitosan Molecular Weight.

    abstract:OBJECTIVES:In this study, central composite factorial design was used for the preparation and optimization of chitosan/Na-alginate hydrogel films containing metformin via solvent evaporation technique. METHODS:Low and high molecular weight (MW) chitosan was used as a polymer in different concentrations while genipin w...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:10.2174/1567201815666180409102459

    authors: Ubaid M,Murtaza G

    更新日期:2018-01-01 00:00:00

  • Particulate systems as adjuvants and carriers for peptide and protein antigens.

    abstract::The most common feature for antigen-delivery systems is their particulate nature. Together with a certain depot effect, it is the particulate nature that primarily dictates whether the antigen-delivery system will be successful in inducing a certain type and strength of immune response. In this article, we will summar...

    journal_title:Current drug delivery

    pub_type: 杂志文章,评审

    doi:10.2174/156720106778559029

    authors: Liang MT,Davies NM,Blanchfield JT,Toth I

    更新日期:2006-10-01 00:00:00

  • Ligand-targeted liposomes for cancer treatment.

    abstract::Selective targeting of ligand-targeted liposomes containing anticancer drugs or therapeutic genes to cell surface receptors expressed on cancer cells is a recognized strategy for improving the therapeutic effectiveness of conventional chemotherapeutics or gene therapeutics. Some recent advances in the field of ligand-...

    journal_title:Current drug delivery

    pub_type: 杂志文章,评审

    doi:10.2174/156720105774370159

    authors: Sapra P,Tyagi P,Allen TM

    更新日期:2005-10-01 00:00:00

  • Advanced Drug Delivery Systems for Transdermal Delivery of Non-Steroidal Anti-Inflammatory Drugs: A Review.

    abstract:BACKGROUND:Transdermal route of delivery of Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) has several advantages over other routes like reduced adverse effects, less systemic absorption, and avoidance of first-pass effect and degradation in the gastrointestinal tract (GIT). Transdermal route is also beneficial for dru...

    journal_title:Current drug delivery

    pub_type: 杂志文章,评审

    doi:10.2174/1567201815666180605114131

    authors: Kumar L,Verma S,Singh M,Chalotra T,Utreja P

    更新日期:2018-01-01 00:00:00

  • Electroporation: an avenue for transdermal drug delivery.

    abstract::The stratum corneum (SC) is a primary rate limiting barrier to permeation of drug molecules through the skin. Small molecular weight lipophilic drugs that are effective at low doses can be effectively delivered by passive transdermal delivery. The SC does not permit passage of polar/hydrophilic and macromolecules. Pas...

    journal_title:Current drug delivery

    pub_type: 杂志文章,评审

    doi:10.2174/156720110791011765

    authors: Charoo NA,Rahman Z,Repka MA,Murthy SN

    更新日期:2010-04-01 00:00:00

  • Medicated Foams and Film Forming Dosage Forms as Tools to Improve the Thermodynamic Activity of Drugs to be Administered Through the Skin.

    abstract::Medicated foams and film forming systems are dosage forms formulated to undergo a controlled metamorphosis when applied on the skin. Indeed, due to the presence of propellant or a particular air-spray foam pump, a liquid can generate foam when applied on the stratum corneum, or a liquid or conventional dosage form can...

    journal_title:Current drug delivery

    pub_type: 杂志文章,评审

    doi:10.2174/1567201816666190118124439

    authors: Gennari CGM,Selmin F,Minghetti P,Cilurzo F

    更新日期:2019-01-01 00:00:00

  • Cancer targeting potential of folate targeted nanocarrier under comparative influence of tretinoin and dexamethasone.

    abstract::The objective of this investigation was aimed to explore the cancer targeting potential of folate conjugated dendrimer (polypropylene imine, PPI) under strategic influence of folate receptor up-regulators (all trans Retinoic acid, ATRA and Dexamethasone, DEXA). The folate conjugated dendrimer nanoconjugate (FPPI) was ...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:10.2174/1567201811310040012

    authors: Dhakad RS,Tekade RK,Jain NK

    更新日期:2013-08-01 00:00:00

  • Artificial organs: a new option for treating osteoarthritis.

    abstract::Osteoarthritis is usually regarded as a localized disease whose optimal treatment is a therapy applied directly to the affected joint. Unfortunately, current local therapies such as repeated intraarticular injections or constant infusions are associated with a higher risk of infection. One way to overcome this would b...

    journal_title:Current drug delivery

    pub_type: 杂志文章,评审

    doi:10.2174/156720107779314839

    authors: Stöve J,Lehmann L,Fickert S,Aigner T,Brenner R

    更新日期:2007-01-01 00:00:00

  • Bupivacaine (S75:R25) Loaded in Nanostructured Lipid Carriers: Factorial Design, HPLC Quantification Method and Physicochemical Stability Study.

    abstract:BACKGROUND:Bupivacaine is the most used local anesthetic in surgical procedures, producing prolonged anesthesia. The major limiting factor for the clinical use of bupivacaine comes from its systemic toxicity. Nanostructured lipid carriers (NLC) are vehicles for sustained drug delivery that are able to minimize the toxi...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:10.2174/1567201814666170726101113

    authors: Da Silva GHR,de Morais Ribeiro LN,Guilherme VA,de Castro SR,Breitkreitz MC,de Paula E

    更新日期:2018-01-01 00:00:00

  • Rheological properties of vaginal hydrophilic polymer gels.

    abstract::The objective of this work was to investigate the main theological features of vaginal hydrophilic polymer gels and to elucidate about the relationship between these characteristics and gels composition, and their general influence in therapeutic/usage purpose. Flow and dynamic oscillatory properties of four commercia...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:10.2174/156720109787048294

    authors: das Neves J,da Silva MV,Gonçalves MP,Amaral MH,Bahia MF

    更新日期:2009-01-01 00:00:00

  • Sterically stabilized polyionic complex nanogels of chitosan lysate and PEG-b-polyglutamic acid copolymer for delivery of irinotecan active metabolite (SN-38).

    abstract:BACKGROUND:Polyionic Complex (PIC) nanogels are promising delivery systems with numerous attractions such as simple, fast, and organic solvent-free particle formation and mild drug loading conditions. Among polyelectrolytes, poly (L-amino acid) copolymers such as poly (ethylene glycol)-block-poly (L-glutamic acid) copo...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:10.2174/1567201817999201103195846

    authors: Salmanpour M,Saeed-Vaghefi M,Abolmaali SS,Tamaddon A

    更新日期:2020-11-03 00:00:00

  • DNA delivery for vaccination and therapeutics through the skin.

    abstract::Cutaneous gene therapy and DNA vaccination are potential applications of plasmid delivery methods where a gene for an antigen or a therapeutic protein is inserted in the plasmid and applied to the skin. However, the delivery of the DNA plasmid is a major challenge due to the unusual physicochemical properties of the D...

    journal_title:Current drug delivery

    pub_type: 杂志文章,评审

    doi:10.2174/156720106775197493

    authors: Foldvari M,Babiuk S,Badea I

    更新日期:2006-01-01 00:00:00

  • Realgar Nanoparticles Inhibit Migration, Invasion and Metastasis in a Mouse Model of Breast Cancer by Suppressing Matrix Metalloproteinases and Angiogenesis.

    abstract:BACKGROUND:Realgar, a traditional Chinese medicine, has shown antitumor efficacy in several tumor types. We previously showed that realgar nanoparticles (nano-realgar) had significant antileukemia, anti-lung cancer and anti-liver cancer effects. In addition, the anti-tumor effects of nanorealgar were significantly bett...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:10.2174/1567201817666200115105633

    authors: Xiaoxia X,Jing S,Dongbin X,Yonggang T,Jingke Z,Yanying Z,Hulai W

    更新日期:2020-01-01 00:00:00

  • Controlled SLN Delivery by Thermoresponsive In-situ Forming Erodible Gels; A Whole-body and Organ Imaging Study.

    abstract:BACKGROUND:Nanoparticles (NPs) suffer from rapid clearance from body and require frequent dosing if long treatment is required. METHOD:In order to solve this problem for solid lipid nanoparticles (SLN) and prolong their action, SLNs were incorporated into thermo-responsive Poloxamer sol-gels and their fate was investi...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:10.2174/1567201815666180201093424

    authors: Dorraj G,Dadashzadeh S,Erfan M,Moghimi HR

    更新日期:2018-01-01 00:00:00

  • Injectable Chitosan/β-Glycerophosphate System for Sustained Release: Gelation Study, Structural Investigation, and Erosion Tests.

    abstract::Hydrogels can constitute reliable delivery systems of drugs, including those based on nucleic acids (NABDs) such as small interfering ribonucleic acid (siRNA). Their nature, structure, and response to physiological or external stimuli strongly influence the delivery mechanisms of entrapped active molecules, and, in tu...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:10.2174/1567201813666160721142202

    authors: Dalmoro A,Abrami M,Galzerano B,Bochicchio S,Barba AA,Grassi M,Larobina D

    更新日期:2017-01-01 00:00:00

  • Phospholipid vesicles as carriers in aquaculture: preparation and stability study of thiamine hydrochloride-loaded liposomes.

    abstract::The aim of this work is to study liposomes as carriers of nutrients and therapeutic agents in aquaculture with Venerupis decussatus and Venerupis pullastra larvae. Multilamellar (MLVs) and large unilamellar (LUVs) vesicles were prepared from a commercial mixture of soy phosphatidylcholine, rich in unsaturated and poly...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:10.2174/1567201043479957

    authors: Lai F,Valenti D,Sinico C,Manconi M,Mendez JB,Fadda AM

    更新日期:2004-04-01 00:00:00

  • Solid Dispersion of Hesperetin Co-crystals Synergistically Attenuates Hepatic Toxicity of Carbon Tetrachloride Oxidative Stress in Rats.

    abstract:BACKGROUND:Hesperetin (HSP) is a low water-soluble flavanone aglycone with low bioavailability. OBJECTIVES:This study aimed at enhancing the hepatoprotective effects of HSP by a combinatory technique based on solid dispersions of co-crystals of HSP. METHODS:Co-crystals were prepared using citric acid, tartaric acid, ...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:10.2174/1567201815666180730141556

    authors: Varshosaz J,Jalali M,Hosseini-Sharifabad A

    更新日期:2018-01-01 00:00:00

  • Oral delivery of insulin with the eligen technology: mechanistic studies.

    abstract::The development of oral insulin using the eligen technology represents a significant advance in insulin administration which is expected to improve the quality of life of diabetic patients. As clinical studies progress, a great deal of interest has focused on the process by which this technology enables insulin absorp...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:10.2174/1567201053586001

    authors: Malkov D,Angelo R,Wang HZ,Flanders E,Tang H,Gomez-Orellana I

    更新日期:2005-04-01 00:00:00

  • Aceclofenac organogels: in vitro and in vivo characterization.

    abstract:PURPOSE:To develop and evaluate the suitability of lecithin organogels containing aceclofenac for topical application and compare its In vitro and In vivo effects with conventionally used hydrogels. METHODS:The components and their concentration necessary for organogels formation were evaluated using phase diagram. So...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:10.2174/156720109787048320

    authors: Shaikh IM,Jadhav SL,Jadhav KR,Kadam VJ,Pisal SS

    更新日期:2009-01-01 00:00:00

  • Design and Development of Thermoreversible Ophthalmic In Situ Hydrogel of Moxifloxacin HCl.

    abstract::Conventional eye drops show relatively low bioavailability due to poor precorneal contact time. In situ hydrogels are of great importance in providing sustained ocular drug delivery. By exhibiting elastic properties they resist ocular drainage of the drug leading to longer contact times. In the present study an in sit...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:10.2174/156720110791560928

    authors: Shastri DH,Prajapati ST,Patel LD

    更新日期:2010-07-01 00:00:00

  • Exploration of Nanoethosomal Transgel of Naproxen Sodium for the Treatment of Arthritis.

    abstract:BACKGROUND:The present work aimed to develop an ethosomal gel of naproxen sodium for the amelioration of rheumatoid arthritis. OBJECTIVE:In the present work, we have explored the potential of ethosomes to deliver naproxen into deeper skin strata. Further, the anti-inflammatory efficacy of naproxen ethosomal formulatio...

    journal_title:Current drug delivery

    pub_type: 杂志文章

    doi:10.2174/1567201817666200724170203

    authors: Anjum F,Zakir F,Verma D,Aqil M,Singh M,Jain P,Mirza MA,Anwer MK,Iqbal Z

    更新日期:2020-01-01 00:00:00