Influence of dissolution medium buffer composition on ketoprofen release from ER products and in vitro-in vivo correlation.

Abstract:

:The purpose of this work was to investigate the influence of dissolution medium composition on the in vitro release of ketoprofen from a series of ER products and the impact of the different buffer media on the in vivo-in vitro (IVIV) relationship. The products investigated were coated micro bead preparations having increasing levels of coating to retard drug release. Four common dissolution media; USP phosphate buffers of pH 7.2 and 6.8, phosphate (modified isotonic) buffer pH 6.8 and a fasted state simulated intestinal fluid without lipid components (FaSSIFLF) of pH 6.5, were employed in the USP 2 apparatus. Release profiles were compared to the corresponding in vivo release profiles, obtained following deconvolution of the plasma level versus time profiles obtained from a 10-subject five-period cross-over study. Despite the relative similarity in composition of the media employed, significant differences in release profiles were observed reflecting media differences in buffer capacity, ionic strength and pH. As a consequence, the quality and shape of the IVIV relationship changed significantly, the only apparent IVIVC incorporating all four ER products, which was non-linear, was obtained using the phosphate (modified isotonic) buffer of pH 6.8. This data was fitted, using a non-linear least squares method, by the equation of Polli et al. [J. Pharm. Sci. 85 (1996) 753] and gave an alpha parameter estimate of 2, consistent with initial dissolution being more rapid in vitro than in vivo. The systematic shift in profiles, particularly with buffer capacity, underlines the sensitivity of IVIV relationship to medium composition and hence the current difficulties in making a rational choice of an appropriate single dissolution medium.

journal_name

Int J Pharm

authors

Corrigan OI,Devlin Y,Butler J

doi

10.1016/s0378-5173(03)00004-8

keywords:

subject

Has Abstract

pub_date

2003-03-26 00:00:00

pages

147-54

issue

2

eissn

0378-5173

issn

1873-3476

pii

S0378517303000048

journal_volume

254

pub_type

杂志文章
  • Green fabricated reduced graphene oxide: evaluation of its application as nano-carrier for pH-sensitive drug delivery.

    abstract::A green and mild approach for the preparation of reduced graphene oxide (rGO) was proposed by using riboflavin-5'-phosphate sodium salt dihydrate as a reducing reagent and stabilizer without any other reagent. The fabricated nano-rGO was systematically evaluated for its application as nano-carrier for pH-sensitive dru...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.10.081

    authors: Ma N,Zhang B,Liu J,Zhang P,Li Z,Luan Y

    更新日期:2015-12-30 00:00:00

  • Enhancing effect of surfactants on fexofenadine.HCl transport across the human nasal epithelial cell monolayer.

    abstract::The effect of various surfactants (sodium cholate, sodium taurocholate, Tween 80 and Poloxamer F68) on enhancing the transepithelial permeability of fexofenadine.HCl was evaluated in a human nasal epithelial cell monolayer model. The cytotoxicity of the surfactants on the human nasal epithelial cells was evaluated by ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.08.043

    authors: Lin H,Gebhardt M,Bian S,Kwon KA,Shim CK,Chung SJ,Kim DD

    更新日期:2007-02-07 00:00:00

  • Modelling nifedipine photodegradation, photostability and actinometric properties.

    abstract:BACKGROUND:The photodegradation of drugs obeying unimolecular mechanisms such as that of nifedipine (NIF) were usually characterised in the literature by zero-, first- and second-order kinetics. This approach has been met with varying success. This paper addresses this issue and proposes a novel approach for unimolecul...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.07.075

    authors: Maafi W,Maafi M

    更新日期:2013-11-01 00:00:00

  • Toward predicting tensile strength of pharmaceutical tablets by ultrasound measurement in continuous manufacturing.

    abstract::An ultrasound measurement system was employed as a non-destructive method to evaluate its reliability in predicting the tensile strength of tablets and investigate the benefits of incorporating it in a continuous line, manufacturing solid dosage forms. Tablets containing lactose, acetaminophen, and magnesium stearate ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.04.064

    authors: Razavi SM,Callegari G,Drazer G,Cuitiño AM

    更新日期:2016-06-30 00:00:00

  • Predicting the gastrointestinal behaviour of modified-release products: utility of a novel dynamic dissolution test apparatus involving the use of bicarbonate buffers.

    abstract::The establishment of physiologically relevant in vitro-in vivo correlations (IV-IVCs) is key for any biorelevant dissolution test. Historically, bicarbonate buffers have produced better correlations than compendial phosphate buffered media, though such tests are usually performed at a constant pH experiment, overlooki...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.09.003

    authors: Merchant HA,Goyanes A,Parashar N,Basit AW

    更新日期:2014-11-20 00:00:00

  • Transcellular brain drug delivery: A review on recent advancements.

    abstract::The blood-brain barrier (BBB) has a pivotal role in maintaining brain homeostasis. It robustly protects the brain parenchyma against the invasion of irrelevant substances, which may interrupt its critical function. From a pharmaceutical point of view, such a barrier may cause central nervous system (CNS) disorders ref...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2020.119582

    authors: Azarmi M,Maleki H,Nikkam N,Malekinejad H

    更新日期:2020-08-30 00:00:00

  • In vitro and in vivo evaluation of potassium chloride sustained release formulation prepared with saturated polyglycolyed glycerides matrices.

    abstract::The aim of the present work was to evaluate the effect of sustained release of potassium chloride semi-solid matrices prepared with different kinds and added amounts of Gelucires by the in vitro dissolution test and in vivo oral absorption study, and compared with a commercial product (slow-K). The results indicating ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00264-8

    authors: Wu PC,Tsai MJ,Huang YB,Chang JS,Tsai YH

    更新日期:2002-08-28 00:00:00

  • Molecular expression and functional activity of sodium dependent multivitamin transporter in human prostate cancer cells.

    abstract::Nutrient transporters expressed on cell membrane have been targeted for enhancing bioavailability of poorly permeable drugs. Sodium dependent multivitamin transporter (SMVT) is once such carrier system, utilized for improving drug targeting to specific tissues. Therefore, the main objective of this study is to charact...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.06.011

    authors: Patel M,Vadlapatla RK,Shah S,Mitra AK

    更新日期:2012-10-15 00:00:00

  • Alkyl glucopyranoside-based niosomes containing methotrexate for pharmaceutical applications: evaluation of physico-chemical and biological properties.

    abstract::We designed novel niosomes based on alkyl glucopyranoside surfactants and containing methotrexate as anticancer drug, to be used in the pharmaceutical field. The effects of surfactants with chains of different length on niosome size and their distribution, drug entrapment efficiencies and in vitro drug release were de...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.09.011

    authors: Muzzalupo R,Tavano L,La Mesa C

    更新日期:2013-12-15 00:00:00

  • Development of a PAT tool for monitoring the Wurster coater performance.

    abstract::Real-time process analytical technology (PAT) is proposed as an effective approach for monitoring the performance of a Wurster coater. The coater was used for coating of 0.78 mm pharmaceutical pellets. The coating solution consisted of Hydroxypropyl methylcellulose/Poly ethylene glycol. During the coating process, sma...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.02.023

    authors: Foroughi-Dahr M,Sotudeh-Gharebagh R,Mostoufi N

    更新日期:2019-04-20 00:00:00

  • A perivascular system releasing sirolimus prevented intimal hyperplasia in a rabbit model in a medium-term study.

    abstract::The main complication of aortocoronary reconstruction with vein grafts is restenosis in the course of time. The aim was to assess the effect of a periadventitial polyester mesh releasing sirolimus on intimal hyperplasia of autologous grafts. We implanted v. jugularis ext. into a. carotis communis in rabbits. The vein ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.02.023

    authors: Skalský I,Szárszoi O,Filová E,Pařízek M,Lytvynets A,Malušková J,Lodererová A,Brynda E,Lisá V,Burdíková Z,Capek M,Pirk J,Bačáková L

    更新日期:2012-05-10 00:00:00

  • Effect of different ratios of high and low molecular weight PLGA blend on the characteristics of pentamidine microcapsules.

    abstract::Two different PLGA samples (Resomer 502 and Resomer 506), either alone or in combinations, were used to prepare microcapsules. Microcapsules were prepared using a double emulsion solvent evaporation technique. The efficiency of encapsulation increased significantly when a mixture of 1 part Resomer 506 and 7 parts Reso...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2003.10.019

    authors: Graves RA,Pamujula S,Moiseyev R,Freeman T,Bostanian LA,Mandal TK

    更新日期:2004-02-11 00:00:00

  • Evaluation of a water-soluble bioadhesive patch for photodynamic therapy of vulval lesions.

    abstract::An innovative bioadhesive patch intended primarily as a vulval drug delivery system and, specifically, as a means to deliver photosensitisers, or their prodrugs, for photodynamic purposes is described. The patch was formulated with a copolymer of methyl vinyl ether and maleic anhydride (PMVE/MA) as a bioadhesive matri...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.11.035

    authors: McCarron PA,Donnelly RF,Zawislak A,Woolfson AD,Price JH,McClelland R

    更新日期:2005-04-11 00:00:00

  • Effect of aqueous solubility of grafted moiety on the physicochemical properties of poly(d,l-lactide) (PLA) based nanoparticles.

    abstract::In order to evaluate the solubility effect of grafted moiety on the physicochemical properties of poly(d,l-lactide) (PLA) based nanoparticles (NPs), two materials of completely different aqueous solubility, polyethylene glycol (PEG) and palmitic acid were grafted on PLA backbone at nearly the same grafting density, 2....

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2009.12.059

    authors: Essa S,Rabanel JM,Hildgen P

    更新日期:2010-03-30 00:00:00

  • Using thin film freezing to minimize excipients in inhalable tacrolimus dry powder formulations.

    abstract::We investigated the feasibility of preparing high-potency tacrolimus dry powder for inhalation using thin film freezing (TFF). We found that using ultra-rapid freezing can increase drug loading up to 95% while maintaining good aerosol performance. Drug loading affected the specific surface area and moisture sorption o...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119490

    authors: Sahakijpijarn S,Moon C,Ma X,Su Y,Koleng JJ,Dolocan A,Williams RO 3rd

    更新日期:2020-08-30 00:00:00

  • Poloxamer-based solid dispersions for oral delivery of docetaxel: Differential effects of F68 and P85 on oral docetaxel bioavailability.

    abstract::Development of an oral docetaxel formulation has been hindered mainly due to its poor solubility and oral bioavailability. The aim of this study was to develop poloxamer F68/P85-based solid dispersions (SDs) for the oral delivery of docetaxel and investigate their in vivo pharmacokinetic impacts on the systemic absorp...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.05.002

    authors: Song CK,Yoon IS,Kim DD

    更新日期:2016-06-30 00:00:00

  • Swelling, melting point reduction and solubility of PEG 1500 in supercritical CO2.

    abstract::The knowledge of the solubility of PEG 1500 as well as the swelling and melting point variation in supercritical CO(2) in a relatively high-pressure range is a necessary prerequisite to set-up pharmaceutical processes dealing with the polymer in the molten state. Experiments carried out in a pressurized view cell indi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.12.048

    authors: Pasquali I,Comi L,Pucciarelli F,Bettini R

    更新日期:2008-05-22 00:00:00

  • Development of enteric-coated fixed dose combinations of amorphous solid dispersions of ezetimibe and lovastatin: Investigation of formulation and process parameters.

    abstract::Enteric-coated fixed-dose combinations of ezetimibe and lovastatin were prepared by fluid bed coating aiming to avoid the acidic conversion of lovastatin to its hydroxyacid derivative. In a two-step process, sucrose beads were layered with a glass solution of ezetimibe, lovastatin and Soluplus®, top-coated with an ent...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.01.053

    authors: Riekes MK,Dereymaker A,Berben P,Augustijns P,Stulzer HK,Van den Mooter G

    更新日期:2017-03-30 00:00:00

  • The role of internal and external stimuli in the rational design of skin-specific drug delivery systems.

    abstract::The concept of skin-specific drug delivery with a spatio-temporal control has just recently received concerns in dermatology. Inspired by the progress in smart materials and their perspective application in medicine science, development of stimuli responsive drug delivery systems with skin-specificity has become possi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2020.120081

    authors: Chen Y,Chen N,Feng X

    更新日期:2021-01-05 00:00:00

  • Oral sustained delivery of ambroxol from in situ-gelling pectin formulations.

    abstract::Gels formed in situ following oral administration of dilute aqueous solutions of pectin (1.0 and 1.5%, w/v) to rats were evaluated as vehicles for the sustained release of the expectorant drug ambroxol hydrochloride. The solutions contained calcium ions in complexed form, which on release in the acidic environment of ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2003.11.027

    authors: Kubo W,Miyazaki S,Dairaku M,Togashi M,Mikami R,Attwood D

    更新日期:2004-03-01 00:00:00

  • Synthesis, characterization, in vitro and in vivo evaluation of PEGylated oridonin conjugates.

    abstract::Oridonin (ORI), a diterpenoid compound with promising antitumor activity, was proved to possess potent antileukemia efficacies in vitro and in vivo recently. However, the development and application of ORI was limited by its poor solubility and rapid plasma clearance. The purpose of this study was to solve these probl...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.08.014

    authors: Shen J,Zhang D,Zhao Z,Jia L,Zheng D,Liu G,Hao L,Zhang Q,Tian X,Li C,Guo H

    更新日期:2013-11-01 00:00:00

  • Physicochemical properties of tamoxifen hemicitrate sesquihydrate.

    abstract::A novel modification of tamoxifen [(Z)-2-[4-(1,2-diphenyl-1-butenyl) phenoxy]-N,N-dimethylethylamine] citrate, tamoxifen hemicitrate hydrate was prepared. The crystalline form was identified and characterized by powder and single crystal X-ray diffractometries, differential scanning calorimetry (DSC), thermal gravimet...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.10.021

    authors: Kojima T,Katoh F,Matsuda Y,Teraoka R,Kitagawa S

    更新日期:2008-03-20 00:00:00

  • Carbon nanotubes from synthesis to in vivo biomedical applications.

    abstract::Owing to their unique and interesting properties, extensive research round the globe has been carried out on carbon nanotubes and carbon nanotubes based systems to investigate their practical usefulness in biomedical applications. The results from these studies demonstrate a great promise in their use in targeted drug...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2016.01.064

    authors: Sajid MI,Jamshaid U,Jamshaid T,Zafar N,Fessi H,Elaissari A

    更新日期:2016-03-30 00:00:00

  • In silico study of patient-specific magnetic drug targeting for a coronary LAD atherosclerotic plaque.

    abstract::Coronary artery disease is the first cause of death across the world. Targeted delivery of therapeutics through controlled release of micro- and nano-particles remains a very capable approach to develop new strategies in treating restenosis and atherosclerotic plaques. In this research, to produce the arterial geometr...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.12.088

    authors: Shamloo A,Amani A,Forouzandehmehr M,Ghoytasi I

    更新日期:2019-03-25 00:00:00

  • The effect of processing variables on the physical characteristics of non-ionic surfactant vesicles (niosomes) formed from a hexadecyl diglycerol ether.

    abstract::Niosomes are vesicles formed by self-assembly of non-ionic surfactants. In this investigation, the effects of processing variables, particularly temperature and sonication, on the physical characteristics and phase transitional behaviour of two niosomal systems based on a hexadecyl diglycerol ether (C(16)G(2)) have be...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(00)00362-8

    authors: Arunothayanun P,Bernard MS,Craig DQ,Uchegbu IF,Florence AT

    更新日期:2000-05-15 00:00:00

  • Triblock copolymers: synthesis, characterization, and delivery of a model protein.

    abstract::The purpose of this study was to synthesize and characterize biodegradable and thermosensitive triblock copolymers for delivering protein at controlled rate in biologically active form for longer duration of time. A series of thermosensitive triblock copolymers with different block lengths (PLGA-PEG-PLGA) were synthes...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.09.026

    authors: Chen S,Pieper R,Webster DC,Singh J

    更新日期:2005-01-20 00:00:00

  • Unexpected differences in dissolution behavior of tablets prepared from solid dispersions with a surfactant physically mixed or incorporated.

    abstract::In a previous study, it was shown that the incorporation of poorly soluble drugs (BCS class II) in sugar glasses could largely increase the drug's dissolution rate [van Drooge, D.J., Hinrichs, W.L.J., Frijlink, H.W., 2004 b. Anomalous dissolution behaviour of tablets prepared from sugar glass-based solid dispersions. ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.07.023

    authors: de Waard H,Hinrichs WL,Visser MR,Bologna C,Frijlink HW

    更新日期:2008-02-12 00:00:00

  • Preparation and characterization of two-phase melt systems of lidocaine.

    abstract::The melting point of lidocaine was significantly lowered when mixed with thymol and/or aqueous ethanol. Mixtures of lidocaine and thymol at ratios within the range of 30:70-70:30 (w:w) became homogeneous oils at 25 degrees C. In a pH 9.2 carbonate buffer containing 25% ethanol, lidocaine (5%, w:w) also liquefied at 25...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(01)00689-5

    authors: Kang L,Jun HW,Mani N

    更新日期:2001-07-03 00:00:00

  • Reflectometric monitoring of the dissolution process of thin polymeric films.

    abstract::Pharmaceutical thin films are versatile drug-delivery platforms i.e. allowing transdermal, oral, sublingual and buccal administration. However, dissolution testing of thin films is challenging since the commonly used dissolution tests for conventional dosage forms correspond rather poorly to the physiological conditio...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.03.028

    authors: Laitinen R,Räty J,Korhonen K,Ketolainen J,Peiponen KE

    更新日期:2017-05-15 00:00:00

  • Thiolated chitosan: development and in vitro evaluation of an oral delivery system for acyclovir.

    abstract::The aim of the study was to develop a novel oral delivery system for the efflux pump substrate acyclovir (ACY) utilizing thiolated chitosan as excipient which is capable of inhibiting P-glycoprotein (P-gp). Three chitosan-4-thiobutylamidine (Chito-TBA) conjugates with increasing molecular mass (Chito-9.4kDa-TBA, Chito...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.07.004

    authors: Palmberger TF,Hombach J,Bernkop-Schnürch A

    更新日期:2008-02-04 00:00:00