Application of continuous twin screw granulation for the metformin hydrochloride extended release formulation.

Abstract:

:This study focuses on evaluating the potential of transferring from a batch process to continuous process for manufacturing of the extended release formulation. Metformin hydrochloride (HCl) was used in the model formulation which was intended to contain the high amount of hydrophilic drug. The effects of barrel temperature, binder type, powder feed rate, and screw speed on granule properties (size and strength) and torque value in twin screw granulation were investigated. Due to the high content of hydrophilic model drug, the granules prepared at a higher temperature with HPMC binding solution had the narrower size distribution and greater strength than the granules prepared with distilled water as a binding solution. After continuous drying and milling steps, the granules (continuous process) satisfied the fundamental purpose of granulation with size and flowability, despite different shape compared with the granules (batch process). Furthermore, there were no significant differences between two granulation processes in tablet properties, such as tablet hardness and in vitro release. The considerations and strategies used in this study to transfer from a batch to continuous process can be applied to other existing formulations based on high shear granulation to enable rapid process transfer in the pharmaceutical industry.

journal_name

Int J Pharm

authors

Kim SH,Hwang KM,Cho CH,Nguyen TT,Seok SH,Hwang KM,Kim JY,Park CW,Rhee YS,Park ES

doi

10.1016/j.ijpharm.2017.07.019

subject

Has Abstract

pub_date

2017-08-30 00:00:00

pages

410-422

issue

1-2

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(17)30618-X

journal_volume

529

pub_type

杂志文章
  • Decylglucoside-based microemulsions for cutaneous localization of lycopene and ascorbic acid.

    abstract::Cutaneous delivery of combinations of antioxidants offers the possibility of enhanced protection against UV-radiation. In this study, we investigated the potential of sugar-based microemulsions containing monoglycerides to promote simultaneous cutaneous delivery of lycopene and ascorbic acid, and increase tissue antio...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.06.016

    authors: Pepe D,Phelps J,Lewis K,Dujack J,Scarlett K,Jahan S,Bonnier E,Milic-Pasetto T,Hass MA,Lopes LB

    更新日期:2012-09-15 00:00:00

  • Acid-base interactions in amorphous solid dispersions of lumefantrine prepared by spray-drying and hot-melt extrusion using X-ray photoelectron spectroscopy.

    abstract::This study investigates drug-excipient interactions in amorphous solid dispersions (ASDs) of the model basic compound lumefantrine (LMN), with five acidic polymers. X-ray photoelectron spectroscopy (XPS) was used to measure the extent of the protonation of the tertiary amine in LMN by the five acidic polymers. The ext...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.06.126

    authors: Song Y,Zemlyanov D,Chen X,Su Z,Nie H,Lubach JW,Smith D,Byrn S,Pinal R

    更新日期:2016-12-05 00:00:00

  • Protein aggregation--pathways and influencing factors.

    abstract::Proteins generally will tend to aggregate under a variety of environmental conditions in comparison with small drug molecules. The extent of aggregation is dependent on many factors that can be broadly classified as intrinsic (primary, secondary, tertiary or quaternary structure) or extrinsic (environment in which pro...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2010.02.025

    authors: Wang W,Nema S,Teagarden D

    更新日期:2010-05-10 00:00:00

  • Enhanced anti-glioblastoma efficacy by PTX-loaded PEGylated poly(ɛ-caprolactone) nanoparticles: In vitro and in vivo evaluation.

    abstract::The aim of this work was to investigate the anti-tumor effect of paclitaxel (PTX)-loaded methoxy poly(ethylene glycol)-poly(ɛ-caprolactone) nanoparticles (MPEG-NP/PTX) against glioblastoma multiforme (GBM). MPEG-NP/PTX was prepared by the emulsion and evaporation technique with particle size of 72.5±2.2nm and did not ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.10.005

    authors: Xin H,Chen L,Gu J,Ren X,Wei Z,Luo J,Chen Y,Jiang X,Sha X,Fang X

    更新日期:2010-12-15 00:00:00

  • Thermoresponsive mesoporous silica nanoparticles as a carrier for skin delivery of quercetin.

    abstract::Recently, mesoporous silica nanoparticles (MSNs) have emerged as promising drug delivery systems able to preserve the integrity of the carried substance and/or to selectively reach a target site; however, they have rarely been explored for skin application. In this study, thermoresponsive MSNs, designed to work at phy...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.07.024

    authors: Ugazio E,Gastaldi L,Brunella V,Scalarone D,Jadhav SA,Oliaro-Bosso S,Zonari D,Berlier G,Miletto I,Sapino S

    更新日期:2016-09-10 00:00:00

  • Development of a buccal bioadhesive nicotine tablet formulation for smoking cessation.

    abstract::Bioadhesive buccal tablet formulations for delivery of nicotine into the oral cavity were developed. Carbomer (Carbopol)974P NF) (CP) and alginic acid sodium salt (NaAlg) were used as bioadhesive polymers in combination with hydroxypropyl methylcellulose (HPMC) at different ratios. Magnesium carbonate was incorporated...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2003.10.040

    authors: Ikinci G,Senel S,Wilson CG,Sumnu M

    更新日期:2004-06-11 00:00:00

  • Enhanced anti-tumor and anti-metastasis therapy for triple negative breast cancer by CD44 receptor-targeted hybrid self-delivery micelles.

    abstract::Tumor growth and metastasis are multistep processes regulated by multiple signaling pathways. The successful treatment of cancer largely depends on the ability to inhibit metastatic process. Multiphase inhibition of metastasis is a promising approach. Here, we described a targeting delivery system which was constructe...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119085

    authors: Yang Y,Long Y,Wang Y,Ren K,Li M,Zhang Z,Xiang B,He Q

    更新日期:2020-03-15 00:00:00

  • Enhanced glioma therapy by synergistic inhibition of autophagy and tyrosine kinase activity.

    abstract::Autophagy is a lysosomal degradation pathway that acts as a cytoprotective mechanism causing treatment resistance in various cancer cells. Recent studies showed that hydroxychloroquine can inhibit the latter step of autophagy and therefore enhance the anti-glioma efficiency of ZD6474, a tyrosine kinase inhibitor. Howe...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.09.007

    authors: Wang X,Qiu Y,Yu Q,Li H,Chen X,Li M,Long Y,Liu Y,Lu L,Tang J,Zhang Z,He Q

    更新日期:2018-01-30 00:00:00

  • In vitro and in vivo studies on ocular vitamin A palmitate cationic liposomal in situ gels.

    abstract::N-trimethyl chitosan (TMC) with different degree of quaternization (DQ) as the coating materials, vitamin A palmitate (VAP)-loaded cationic liposomes dispersed in thermo-sensitive in situ gels (ISG) with poloxamer 407 (P407) as the base were prepared in this study. VAP-loaded liposomes (VAPL) were prepared using a fil...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:

    authors: He W,Guo X,Feng M,Mao N

    更新日期:2013-12-31 00:00:00

  • Comparison of different zeolite framework types as carriers for the oral delivery of the poorly soluble drug indomethacin.

    abstract::Microporous zeolites of distinct framework types, textural properties and crystal morphologies namely BEA, ZSM and NaX, have been employed as carriers to assess their effect on modulating the dissolution behavior of a BCS II model drug (indomethacin). Preparation of the loaded carriers via the incipient wetness method...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.05.061

    authors: Karavasili C,Amanatiadou EP,Kontogiannidou E,Eleftheriadis GK,Bouropoulos N,Pavlidou E,Kontopoulou I,Vizirianakis IS,Fatouros DG

    更新日期:2017-08-07 00:00:00

  • Evaluation of P(L)LA-PEG-P(L)LA as processing aid for biodegradable particles from gas saturated solutions (PGSS) process.

    abstract::A series of biodegradable P(L)LA-PEG1.5 kDa-P(L)LA copolymers have been synthesized and compared as processing aid versus Poloxamer 407 (PEO-PPO-PEO), in the formulation of protein encapsulated microparticles, using supercritical carbon dioxide (scCO2). Bovine serum albumin (BSA) loaded microcarriers were prepared app...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.04.031

    authors: Perinelli DR,Bonacucina G,Cespi M,Naylor A,Whitaker M,Palmieri GF,Giorgioni G,Casettari L

    更新日期:2014-07-01 00:00:00

  • Investigation of properties and recrystallisation behaviour of amorphous indomethacin samples prepared by different methods.

    abstract::The aim of this study was to investigate if amorphous indomethacin samples, prepared using different preparation methods, exhibit different structural and kinetic characteristics and if these differences can be correlated to their physical stability (time to crystallisation). Samples were prepared by melt quenching, s...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.12.019

    authors: Karmwar P,Graeser K,Gordon KC,Strachan CJ,Rades T

    更新日期:2011-09-30 00:00:00

  • Prolonged analgesic effect of PLGA-encapsulated bee venom on formalin-induced pain in rats.

    abstract::To enhance the medicinal activity of bee venom (BV) acupuncture, bee venom was loaded into biodegradable poly(D,L-lactide-co-glycolide) nanoparticles (BV-PLGA-NPs) by a water-in-oil-in-water-emulsion/solvent-evaporation technique. Rat formalin tests were performed after subcutaneous injection of BV-PLGA-NPs to the Zus...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2009.06.034

    authors: Jeong I,Kim BS,Lee H,Lee KM,Shim I,Kang SK,Yin CS,Hahm DH

    更新日期:2009-10-01 00:00:00

  • Cytotoxicity and permeability enhancement of Capmul®MCM in nanoemulsion formulation.

    abstract::This study aimed to investigate the following factors affecting the cytotoxicity of Capmul®MCM (C8/10MD) in self-emulsified nanoemulsions (SENs): concentration, triglycerides, and droplet size, and how these factors influence permeability of lipid droplets. Two triglycerides (C8T and C18T) and six formulations were us...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.03.010

    authors: Bunchongprasert K,Shao J

    更新日期:2019-04-20 00:00:00

  • Investigation into the influence of polymeric stabilizing excipients on inter-particulate forces in pressurised metered dose inhalers.

    abstract::Colloid probe atomic force microscopy (AFM) was utilised to quantify the cohesive forces of salbutamol sulphate in a model non-pressurised fluorinated liquid (mHFA), in the presence of increasing concentrations of poly(ethylene glycol) (PEG; molecular weight (MW) 200, 400 and 600). In addition, samples of PEG 400 (0.0...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.04.016

    authors: Traini D,Young PM,Rogueda P,Price R

    更新日期:2006-08-31 00:00:00

  • Process and formulation characterizations of the thermal adhesion granulation (TAG) process for improving granular properties.

    abstract::In this study, we demonstrate the feasibility of using the thermal adhesion granulation (TAG) method to improve granular properties for preparing highly compressible excipients as direct tabletting aids. The TAG method subjects a mixture containing excipients, such as microcrystalline cellulose (MCC), lactose, starch,...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.02.002

    authors: Lin HL,Ho HO,Chen CC,Yeh TS,Sheu MT

    更新日期:2008-06-05 00:00:00

  • Design and characterization of a perivascular PLGA coated PET mesh sustaining the release of atorvastatin for the prevention of intimal hyperplasia.

    abstract::Following vascular bypass interventions, autologous saphenous vein grafts are prone to fail due to intimal hyperplasia development. An atorvastatin (ATV)-eluting tubular mesh coated with poly(d,l-lactide-co-glycolisde) acid (PLGA) was designed for perivascular application, in order to prevent the development of this p...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.12.026

    authors: Mylonaki I,Trosi O,Allémann E,Durand M,Jordan O,Delie F

    更新日期:2018-02-15 00:00:00

  • Drug release from and mechanical properties of press-coated tablets with hydroxypropylmethylcellulose acetate succinate and plasticizers in the outer shell.

    abstract::Dissolution profiles of diltiazem hydrochloride (DIL) contained in core tablets from press-coated (PC) tablets with hydroxypropylmethylcellulose acetate succinate (HPMCAS) and plasticizers-adsorbent in the outer shell were investigated. Although, on the addition of triethyl citrate (TEC), triacetin (TA), and acetyltri...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(01)00578-6

    authors: Fukui E,Miyamura N,Yoneyama T,Kobayashi M

    更新日期:2001-04-17 00:00:00

  • Characterisation and stability studies of a hydrophilic decapeptide in different adjuvant drug delivery systems: a comparative study of PLGA nanoparticles versus chitosan-dextran sulphate microparticles versus DOTAP-liposomes.

    abstract::Poly[lactic-co-glycolide] (PLGA) nanoparticles, chitosan-dextran sulphate microparticles, and DOTAP-liposomes were prepared as vaccine adjuvants and drug carriers for a small hydrophilic model peptide, and their different physico-chemical properties (size, PDI, zeta-potential, pH-value and peptide loading) were invest...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.09.011

    authors: Wieber A,Selzer T,Kreuter J

    更新日期:2011-12-12 00:00:00

  • Transferosomes as nanocarriers for drugs across the skin: Quality by design from lab to industrial scale.

    abstract::Transferosomes, also known as transfersomes, are ultradeformable vesicles for transdermal applications consisting of a lipid bilayer with phospholipids and an edge activator and an ethanol/aqueous core. Depending on the lipophilicity of the active substance, it can be encapsulated within the core or amongst the lipid ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2019.118817

    authors: Fernández-García R,Lalatsa A,Statts L,Bolás-Fernández F,Ballesteros MP,Serrano DR

    更新日期:2020-01-05 00:00:00

  • Buccal permeation of [D-Ala(2), D-Leu(5)]enkephalin from liquid crystalline phases of glyceryl monooleate.

    abstract::The ex vivo buccal permeability of a [D-Ala(2), D-Leu(5)]enkephalin (DADLE) and glyceryl monooleate (GMO) was examined from the cubic and lamellar liquid crystalline phases of GMO and aqueous phosphate-buffered saline (pH 7.4, PBS) solution across excised porcine buccal mucosa mounted in a Franz cell. GMO was released...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00357-9

    authors: Lee J,Kellaway IW

    更新日期:2000-02-15 00:00:00

  • Design, development and evaluation of PEGylated rhGH with preserving its bioactivity at highest level after modification.

    abstract::Modification of recombinant proteins with polyethylene-glycol (PEG) can improve their pharmacokinetic properties, although their bioactivity may be reduced after PEGylation due to structural changes. In this study, simultaneous optimization of PEGylation efficiency and preserved bioactivity of recombinant human growth...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.12.034

    authors: Karbasian M,Kouchakzadeh H,Anamaghi PN,Sefidbakht Y

    更新日期:2019-02-25 00:00:00

  • alpha-Cyclodextrin/oil beads: an innovative self-assembling system.

    abstract::The aim of this work was to characterise a new type of particulate system, named beads, prepared by a straightforward technique starting from a mixture of alpha-cyclodextrin aqueous solution and soybean oil without the use of any organic solvent or surface-active agent. Mechanisms involved in bead formation were also ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.02.034

    authors: Bochot A,Trichard L,Le Bas G,Alphandary H,Grossiord JL,Duchêne D,Fattal E

    更新日期:2007-07-18 00:00:00

  • Arrhenius activation energy of damage to catalase during spray-drying.

    abstract::The inactivation of catalase during spray-drying over a range of outlet gas temperatures could be closely represented by the Arrhenius equation. From this an activation energy for damage to the catalase could be calculated. The close fit to Arrhenius suggests that the thermally-induced part of inactivation of the cata...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.04.078

    authors: Schaefer J,Lee G

    更新日期:2015-07-15 00:00:00

  • Evaluation and structure-activity relationship of synthesized cyclohexanol derivatives on percutaneous absorption of ketoprofen using artificial neural network.

    abstract::The effect of 35 newly synthesized O-ethylmenthol (MET) derivatives on percutaneous absorption of ketoprofen was investigated in rats. In order to understand the relationship between the structure of compounds and promoting activity (structure-activity relationship), an artificial neural network (ANN) was employed. In...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(00)00608-6

    authors: Obata Y,Li CJ,Fujikawa M,Takayama K,Sato H,Higashiyama K,Isowa K,Nagai T

    更新日期:2001-01-16 00:00:00

  • Biological properties of low molecular mass peptide dendrimers.

    abstract::A series of new, low molecular mass, lysine-based peptide dendrimers with varying distribution of cationic and aromatic groups in the structure were synthesized. They expressed antimicrobial activity against Gram-positive (Staphylococcus aureus) and Gram-negative (Escherichia coli) bacteria as well as against fungal p...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.10.039

    authors: Klajnert B,Janiszewska J,Urbanczyk-Lipkowska Z,Bryszewska M,Shcharbin D,Labieniec M

    更新日期:2006-02-17 00:00:00

  • Plasticizer di(2-ethylhexyl)phthalate (DEHP) release in wet-primed extracorporeal membrane oxygenation (ECMO) circuits.

    abstract::A wet-primed ready-to-use extracorporeal membrane oxygenation (ECMO) circuit is used in some centres for rapid deployment of ECMO during cardiopulmonary resuscitation. Yet, the potential release of plasticizer di(2-ethylhexyl)phthalate (DEHP) from the polyvinyl chloride tubing in the circuit during storage is a concer...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.01.030

    authors: Han J,Beeton A,Long P,Karimova A,Robertson A,Cross N,Smith L,O'Callaghan M,Goldman A,Brown K,Tuleu C

    更新日期:2005-04-27 00:00:00

  • Gelation of the internal core of liposomes as a strategy for stabilization and modified drug delivery I. Physico-chemistry study.

    abstract::Since the application of nanotechnology to drug delivery, both polymer-based and lipid-based nanocarriers have demonstrated clinical benefits, improving both drug efficacy and safety. However, to further address the challenges of the drug delivery field, hybrid lipid-polymer nanocomposites have been designed to merge ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119467

    authors: Petralito S,Paolicelli P,Nardoni M,Trilli J,Di Muzio L,Cesa S,Relucenti M,Matassa R,Vitalone A,Adrover A,Casadei MA

    更新日期:2020-07-30 00:00:00

  • WITHDRAWN: Microfabrication of dissolvable, swellable, and biodegradable polymeric microneedle arrays.

    abstract::This article has been withdrawn at the request of the authors. The Publisher apologizes for any inconvenience this may cause. The full Elsevier Policy on Article Withdrawal can be found at http://www.elsevier.com/locate/withdrawalpolicy. ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.11.046

    authors: Demir YK,Akan Z,Kerimoglu O

    更新日期:2012-12-20 00:00:00

  • Mathematical modeling of the fluid dynamics in the flow-through cell.

    abstract::The fluid dynamics in the flow-through cell (USP apparatus 4) has been predicted using the mathematical modeling approach of computational fluid dynamics (CFD). The degree to which flow structures in this apparatus can be qualified as 'ideal' both spatially and temporally has been assessed. The simulations predict the...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2009.04.012

    authors: Kakhi M

    更新日期:2009-07-06 00:00:00