Pluronic F127-g-poly(acrylic acid) copolymers as in situ gelling vehicle for ophthalmic drug delivery system.

Abstract:

:To prolong the precorneal resident time and improve ocular bioavailability of the drug, Pluronic F127-g-poly(acrylic acid) copolymers were studied as in situ gelling vehicle for ophthalmic drug delivery system. The rheological properties and in vitro drug release of Pluronic-g-PAA copolymer gels were investigated. The rheogram and in vitro drug release studies indicated that the drug release rates decreased as acrylic acid/Pluronic molar ratio and copolymer solution concentration increased. But the drug concentration had no obvious effect on drug release. The release rates of the drug from such copolymer gels were mainly dependent on the gel dissolution. In vivo resident experiments showed the drug resident time and the total resident amount in rabbit's conjunctiveal sac increased by 5.0 and 2.6 folds for in situ gel, compared with eye drops. The decreased loss angle at body temperature and prolonged precorneal resident time also indicated that the copolymer gels had bioadhesive properties. These in vivo experimental results, along with the rheological properties and in vitro drug release studies, demonstrated that in situ gels containing Pluronic-g-PAA copolymer may significantly prolong the drug resident time and thus improve bioavailability. Pluronic-g-PAA copolymer can be a promising in situ gelling vehicle for ophthalmic drug delivery system.

journal_name

Int J Pharm

authors

Ma WD,Xu H,Wang C,Nie SF,Pan WS

doi

10.1016/j.ijpharm.2007.09.005

subject

Has Abstract

pub_date

2008-02-28 00:00:00

pages

247-56

issue

1-2

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(07)00757-0

journal_volume

350

pub_type

杂志文章
  • Preparation of MPEG-PLA nanoparticle for honokiol delivery in vitro.

    abstract::Honokiol (HK) shows potential application in cancer treatment, but its poor water solubility restricts clinical application greatly. In this paper, monomethoxy poly(ethylene glycol)-poly(lactic acid) (MPEG-PLA) was synthesized by ring-opening polymerization and processed into nanoparticle for honokiol delivery. Chemic...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2009.11.014

    authors: Zheng X,Kan B,Gou M,Fu S,Zhang J,Men K,Chen L,Luo F,Zhao Y,Zhao X,Wei Y,Qian Z

    更新日期:2010-02-15 00:00:00

  • Examination of oxidized cellulose as a macromolecular prodrug carrier: preparation and characterization of an oxidized cellulose-phenylpropanolamine conjugate.

    abstract::The purpose of this study was to investigate the use of 6-carboxycellulose (OC), a biocompatible and bioresorbable polymer, as a prodrug carrier for amine drugs. Phenylpropanolamine hydrochloride (PPA.HCl) was used as a model drug. OC and PPA were reacted in dimethylformamide (DMF) in the presence of 1,3-dicyclohexylc...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(01)00725-6

    authors: Zhu L,Kumar V,Banker GS

    更新日期:2001-07-31 00:00:00

  • Fabrication of inhalable spore like pharmaceutical particles for deep lung deposition.

    abstract::An innovative strategy of fabricating uniform spore like drug particles to improve pulmonary drug delivery efficiency was disclosed in the present study. Spore like particles were prepared through combination of high gravity controlled precipitation and spray drying process with insulin as model drug first, showing ro...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.03.044

    authors: Shen ZG,Chen WH,Jugade N,Gao LY,Glover W,Shen JY,Yun J,Chen JF

    更新日期:2012-07-01 00:00:00

  • Protease-functionalized mucus penetrating microparticles: In-vivo evidence for their potential.

    abstract::The focus of the current study was to explore whether immobilization of proteases to microparticles could result in their enhanced penetration into mucus. The proteases papain (PAP) and bromelain (BROM) were covalently attached to a polyacrylate (PAA; Carbopol 971P) via amide bond formation based on carbodiimide react...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.08.114

    authors: Mahmood A,Laffleur F,Leonaviciute G,Bernkop-Schnürch A

    更新日期:2017-10-30 00:00:00

  • Effect of the combination of organic and inorganic filters on the Sun Protection Factor (SPF) determined by in vitro method.

    abstract::This paper describes the effect on Sun Protection Factor (SPF) of the combination of inorganic and organic filters in sunscreen products as determined by an in vitro method. O/W emulsions containing inorganic filters, such as titanium dioxide and zinc oxide, combined with 18 EU-authorized UV-B organic filters were tes...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.05.047

    authors: El-Boury S,Couteau C,Boulande L,Paparis E,Coiffard LJ

    更新日期:2007-08-01 00:00:00

  • Spherical agglomerates of lactose with enhanced mechanical properties.

    abstract::The aim of this study was to prepare spherical agglomerates of lactose and to evaluate their physicochemical properties, flow properties, particle friability and compaction properties, and to compare them to commercially available types of lactose for direct compression (spray-dried, granulated and anhydrous β-lactose...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.11.040

    authors: Lamešić D,Planinšek O,Lavrič Z,Ilić I

    更新日期:2017-01-10 00:00:00

  • Cold flow of estradiol transdermal systems: influence of drug loss on the in vitro flux and drug transfer across human epidermis.

    abstract::The objective was to quantify drug loss due to cold flow (CF) in marketed estradiol transdermal drug delivery systems (TDDS), and study its influence on the in vitro flux and drug transfer across contacting skin. TDDS samples (products-A and B) were induced with CF at 25 and 32°C/60% RH by applying 1-kg force for 72h....

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.10.013

    authors: Krishnaiah YS,Yang Y,Hunt RL,Khan MA

    更新日期:2014-12-30 00:00:00

  • Needle-free intravaginal DNA vaccination using a stearoyl oligopeptide carrier promotes local gene expression and immune responses.

    abstract::The vaginal mucosa is the most common site of infection for viruses that are transmitted through heterosexual intercourse, including human immunodeficiency virus and papillomavirus. Thus, in order to prevent or respond to these infections, strong vaginal immunity is required as the first line of defense. We previously...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.02.018

    authors: Kanazawa T,Tamura T,Yamazaki M,Takashima Y,Okada H

    更新日期:2013-04-15 00:00:00

  • Data-smart machine learning methods for predicting composition-dependent Young's modulus of pharmaceutical compacts.

    abstract::The ability to predict mechanical properties of compacted powder blends of Active Pharmaceutical Ingredients (API) and excipients solely from component properties can reduce the amount of 'trial-and-error' involved in formulation design. Machine Learning (ML) can reduce model development time and effort with the imper...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.120049

    authors: Thomas S,Palahnuk H,Amini H,Akseli I

    更新日期:2021-01-05 00:00:00

  • Continuous direct compression as manufacturing platform for sustained release tablets.

    abstract::This study presents a framework for process and product development on a continuous direct compression manufacturing platform. A challenging sustained release formulation with high content of a poorly flowing low density drug was selected. Two HPMC grades were evaluated as matrix former: standard Methocel CR and direc...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.01.010

    authors: Van Snick B,Holman J,Cunningham C,Kumar A,Vercruysse J,De Beer T,Remon JP,Vervaet C

    更新日期:2017-03-15 00:00:00

  • The influence of the physicochemical characteristics and pharmacokinetic properties of selected NSAID's on their transdermal absorption.

    abstract::The purpose of this study was to determine the plasma concentrations of selected NSAIDs after topical gel administration and to determine the influence of the physicochemical characteristics of these drugs on transdermal absorption. Plasma concentrations of the drugs were determined using high performance liquid chrom...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00340-3

    authors: Beetge E,du Plessis J,Müller DG,Goosen C,van Rensburg FJ

    更新日期:2000-01-05 00:00:00

  • Polyamine metabolism-based dual functional gene delivery system to synergistically inhibit the proliferation of cancer.

    abstract::Polyamine content, which is associated with tumor growth, can be regulated by ornithine decarboxylase (ODC) and S-adenosyl methionine decarboxylase (SAMDC), two key enzymes in polyamine biosynthesis. Here we aim to develop a pH-responsive cationic poly(agmatine) based on a polyamine analogue-agmatine that can dually f...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.04.039

    authors: Cui PF,Xing L,Qiao JB,Zhang JL,He YJ,Zhang M,Lyu JY,Luo CQ,Jin L,Jiang HL

    更新日期:2016-06-15 00:00:00

  • Understanding die fill variation during mini-tablet production.

    abstract::Reproducibility of die fill during tablet production is critical to ensure consistent tablet drug content and mechanical attributes. In the production of mini-tablets, tablets smaller than 6mm, achievement of uniform die fill is much more challenging. Powder flow is often associated with die fill accuracy but this rel...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.10.042

    authors: Goh HP,Heng PWS,Liew CV

    更新日期:2017-12-20 00:00:00

  • In-situ single pass intestinal permeability and pharmacokinetic study of developed Lumefantrine loaded solid lipid nanoparticles.

    abstract::The present investigation aims to develop lumefantrine loaded binary solid lipid nanoparticles (LF-SLNs) to improve its poor and variable oral bioavailability. The oral bioavailability of LF is poor and variable due to its limited aqueous solubility and P-gp mediated efflux occurring in small intestine. LF-SLNs were p...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.10.064

    authors: Garg A,Bhalala K,Tomar DS,Wahajuddin

    更新日期:2017-01-10 00:00:00

  • Solid lipid nanoparticles as potential tools for gene therapy: in vivo protein expression after intravenous administration.

    abstract::Naked plasmid DNA is a powerful tool for gene therapy, but it is rapidly eliminated from the circulation after intravenous administration. Therefore, the development of optimized DNA delivery systems is necessary for its successful clinical use. Solid lipid nanoparticles (SLNs) have demonstrated transfection capacity ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2009.10.020

    authors: del Pozo-Rodríguez A,Delgado D,Solinís MA,Pedraz JL,Echevarría E,Rodríguez JM,Gascón AR

    更新日期:2010-01-29 00:00:00

  • Herceptin-functionalized pure paclitaxel nanocrystals for enhanced delivery to HER2-postive breast cancer cells.

    abstract::The objective of this study was to prepare Herceptin (HCT)-functionalized paclitaxel nanocrystals and evaluated their cell-specific interactions, cellular accumulation, and growth inhibition in HER2-positve breast cancer cells as a tumor-targeted delivery module. Paclitaxel (PTX) was fabricated in the form of nanocrys...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.09.067

    authors: Noh JK,Naeem M,Cao J,Lee EH,Kim MS,Jung Y,Yoo JW

    更新日期:2016-11-20 00:00:00

  • Cyclosporine A-loaded lipid nanoparticles in inflammatory bowel disease.

    abstract::Cyclosporine A (CsA) is a well-known immunosuppressive agent used as rescue therapy in severe steroid-refractory ulcerative colitis (UC). However, toxicity issues associated with CsA when administered in its commercially available formulations have been reported in clinical practice. Since nanotechnology has been prop...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.03.012

    authors: Guada M,Beloqui A,Alhouayek M,Muccioli GG,Dios-Viéitez Mdel C,Préat V,Blanco-Prieto MJ

    更新日期:2016-04-30 00:00:00

  • Synthesis and characterization of polyurethane and poly(ether urethane) nanocapsules using a new technique of interfacial polycondensation combined to spontaneous emulsification.

    abstract::Polyurethane polymers and poly(ether urethane) copolymers were chosen as drug carriers for alpha-tocopherol. This active ingredient is widely used as a strong antioxidant in many medical and cosmetic applications, but is rapidly degraded, because of its light, heat and oxygen sensitivity. Polyurethane and poly(ether u...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2003.09.025

    authors: Bouchemal K,Briançon S,Perrier E,Fessi H,Bonnet I,Zydowicz N

    更新日期:2004-01-09 00:00:00

  • Evaluation of collagen and methylated collagen as gene carriers.

    abstract::This study explores the potential of DNA complexes prepared with methylated collagen (MC) and unmodified native collagen (NC) to deliver genes into cells. The physicochemical properties and transfection abilities of these two types of complexes are studied in parallel. MC was prepared by methylation of the carboxyl gr...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.04.014

    authors: Wang J,Lee IL,Lim WS,Chia SM,Yu H,Leong KW,Mao HQ

    更新日期:2004-07-26 00:00:00

  • Electrically controlled release of salicylic acid from poly(p-phenylene vinylene)/polyacrylamide hydrogels.

    abstract::The apparent diffusion coefficients, Dapp, and the release mechanisms of salicylic acid from salicylic acid-loaded polyacrylamide hydrogels, SA-loaded PAAM, and salicylic acid-doped poly(phenylene vinylene)/polyacrylamide hydrogels, SA-doped PPV/PAAM, were investigated. In the absence of an electric field, the diffusi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.12.032

    authors: Niamlang S,Sirivat A

    更新日期:2009-04-17 00:00:00

  • Design and evaluation of an aerosol infection chamber for small animals.

    abstract::In this report, we describe the design of an aerosol exposure chamber to reproducibly produce uniformly distributed clouds of droplet nuclei. The device can deliver desired number of bacilli (20-2000) in lungs of mice. All safety measures to handle infectious bacteria have been incorporated in the design and it is con...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(03)00023-1

    authors: Bhaskar S,Upadhyay P

    更新日期:2003-04-14 00:00:00

  • Size-dependency of nanoparticle-mediated gene transfection: studies with fractionated nanoparticles.

    abstract::Nanoparticles formulated from biodegradable polymers such as poly (lactic acid) and poly (D,L-lactide-co-glycolide) (PLGA) are being extensively investigated as non-viral gene delivery systems due to their sustained release characteristics and biocompatibility. PLGA nanoparticles for DNA delivery are mainly formulated...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00315-0

    authors: Prabha S,Zhou WZ,Panyam J,Labhasetwar V

    更新日期:2002-09-05 00:00:00

  • Effect of varying the restriction degree of 4-aminopyridine release from HPMC matrices on the mechanism controlling the process.

    abstract::Among different technological variables that influence drug release from hydrophilic matrices, different proportions of the polymer and a water-soluble excipient have been used to control the drug release properties. These variables were used to modify the drug release rate and to examine its effect on the mechanism c...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(03)00150-9

    authors: Martínez-González I,Villafuerte-Robles L

    更新日期:2003-05-12 00:00:00

  • Downstream drug product processing of itraconazole nanosuspension: Factors influencing drug particle size and dissolution from nanosuspension-layered beads.

    abstract::There is more research required to broaden the knowledge on the downstream processing of nanosuspensions into solid oral dosage forms, especially for coated nanosuspensions onto beads as carriers. This study focuses on bead layering as one approach to solidify nanosuspensions. The aim was to systematically investigate...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.04.012

    authors: Parmentier J,Tan EH,Low A,Möschwitzer JP

    更新日期:2017-05-30 00:00:00

  • In vivo efficacy of paclitaxel-loaded injectable in situ-forming gel against subcutaneous tumor growth.

    abstract::Injectable in situ-forming gels have received considerable attention as localized drug delivery systems. Here, we examined a poly(ethylene glycol)-b-polycaprolactone (MPEG-PCL) diblock copolymer gel as an injectable drug depot for paclitaxel (Ptx). The copolymer solution remained liquid at room temperature and rapidly...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.03.033

    authors: Lee JY,Kim KS,Kang YM,Kim ES,Hwang SJ,Lee HB,Min BH,Kim JH,Kim MS

    更新日期:2010-06-15 00:00:00

  • Effect of cholesterol and temperature on the elastic properties of niosomal membranes.

    abstract::The mechanical characteristics of non-ionic bilayer membranes composed of sorbitan monostearate, cholesterol and poly-24-oxyethylene cholesteryl were studied by measuring the modulus of surface elasticity (mu), a measure of membrane strength, as a function of cholesterol content and temperature. The modulus of surface...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.05.009

    authors: Nasseri B

    更新日期:2005-08-26 00:00:00

  • An in vitro kinetic method for detection of precipitation of poorly soluble drugs.

    abstract::A simple in vitro method for the detection of precipitation using 96-well microplates and a SpectraMax Plus microtiter plate reader has been developed and described. The method requires only small amount of drug and is, therefore, potentially applicable in early pre-formulation. The method is based on opacity changes ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.08.012

    authors: Wu Z,Tucker IG,Razzak M,Medlicott NJ

    更新日期:2005-11-04 00:00:00

  • pH sensitive alginate-guar gum hydrogel for the controlled delivery of protein drugs.

    abstract::Design of a pH sensitive alginate-guar gum hydrogel crosslinked with glutaraldehyde was done for the controlled delivery of protein drugs. Alginate is a non-toxic polysaccharide with favorable pH sensitive properties for intestinal delivery of protein drugs. Drug leaching during hydrogel preparation and rapid dissolut...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.11.009

    authors: George M,Abraham TE

    更新日期:2007-04-20 00:00:00

  • Comparative study of liposomes, ethosomes and transfersomes as carriers for enhancing the transdermal delivery of diflunisal: In vitro and in vivo evaluation.

    abstract::The current study aimed to develop an effective transdermal nanovesicular carrier of diflunisal that provides enhanced delivery through the skin. Two types of nanovesicles, ethosomes and transfersomes, were investigated and compared to conventional liposomes. Ethosomes with variable ethanol contents (10, 30 and 50%) a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.04.001

    authors: Abd El-Alim SH,Kassem AA,Basha M,Salama A

    更新日期:2019-05-30 00:00:00

  • Investigating permeability related hurdles in oral delivery of 11-keto-β-boswellic acid.

    abstract::11-Keto-β-boswellic acid (KBA) is an important and potent boswellic acids responsible for anti-inflammatory action of Boswellia extract. However, its pharmaceutical development has been severely limited by its poor oral bioavailability. The present work aims to investigate the permeability related hurdles in oral deli...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.01.019

    authors: Bagul P,Khomane KS,Bansal AK

    更新日期:2014-04-10 00:00:00