Influence of pH, buffer species, and storage temperature on physicochemical stability of a humanized monoclonal antibody LA298.

Abstract:

:The purpose of this work is to study the effect of pH, buffer species, and temperature on the physicochemical stability of a humanized monoclonal antibody LA298. The study was carried out in solution state of the antibody in the presence of different buffer species at different pH values and storage temperature. No significant changes in total protein content were observed for any of the solutions with different buffers at different pH values when stored for 8 weeks at both 5 degrees C and 25 degrees C or at 37 degrees C for 1 week. Known asparagines (Asn55) deamidation of LA298 was found to be dependent on pH, buffer type, and temperature. The estimated rate constant of the double heavy chain Asn55 deamidation in phosphate buffer at pH 6.5 and 7.0 was much higher than that in citrate buffer under the same storage conditions. However, comparable results were obtained for single heavy chain Asn55 deamidation in citrate and phosphate buffer. Aggregation of LA298 was not significant for samples at different pH values, buffers, and temperatures as the monomer of LA298 decreased dramatically over time. Less decrease in monomeric LA298 was observed in citrate buffer, pH 5.0-5.5. In conclusion, to minimize deamidation and loss of LA298 monomer, it is important to optimize its solution pH, buffer species, and storage temperature.

journal_name

Int J Pharm

authors

Zheng JY,Janis LJ

doi

10.1016/j.ijpharm.2005.10.024

keywords:

subject

Has Abstract

pub_date

2006-02-03 00:00:00

pages

46-51

issue

1-2

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(05)00707-6

journal_volume

308

pub_type

杂志文章
  • Freeze-dried cake structural and physical heterogeneity in relation to freeze-drying cycle parameters.

    abstract::Freeze-drying is the preferred method to manufacture proteins in their solid state thus the understanding of the relationship between cycle parameters and cake properties remains of great interest. The present study aims to investigate the influence of the freezing conditions in the material properties at different la...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119891

    authors: Badal Tejedor M,Fransson J,Millqvist-Fureby A

    更新日期:2020-11-30 00:00:00

  • Lysozyme-loaded, electrospun chitosan-based nanofiber mats for wound healing.

    abstract::In this study, a blend mixture of chitosan-ethylenediaminetetraacetic acid (CS 2 wt%-EDTA) at a weight ratio of 30/70 and polyvinyl alcohol (PVA) solution (10 wt%) was electrospun to produce fibrous mats with lysozyme (10, 20 and 30 wt%) used for wound healing. The morphology and diameter of the electrospun fiber mats...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.02.010

    authors: Charernsriwilaiwat N,Opanasopit P,Rojanarata T,Ngawhirunpat T

    更新日期:2012-05-10 00:00:00

  • Ibuprofen-phospholipid solid dispersions: improved dissolution and gastric tolerance.

    abstract::Solid dispersions of ibuprofen with various phospholipids were prepared, and the effect of phospholipids on the in vitro dissolution and in vivo gastrointestinal toxicity of ibuprofen was evaluated. Most phospholipids improved the dissolution of ibuprofen; dimyristoylphosphatidyl-glycerol (DMPG) had the greatest effec...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.11.011

    authors: Hussain MD,Saxena V,Brausch JF,Talukder RM

    更新日期:2012-01-17 00:00:00

  • Characterization of nifedipine microparticles prepared by hot air coating technique.

    abstract::In the present work, the Hot Air Coating (HAC) technique was used to prepare microparticulate systems containing nifedipine. Binary mixtures constituting of nifedipine and cetearyl alcohol (CA) in different proportions (30:70, 50:50, 70:30) were studied: they were homogenized by mixing or milling before spray treatmen...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.01.010

    authors: Giovannelli L,Bellomi S,Pattarino F,Albertini B

    更新日期:2005-04-11 00:00:00

  • Synthesis, characterization and bioevaluation of drug-collagen hybrid materials for biomedical applications.

    abstract::This work presents a study based on the preparation and characterization of drug-collagen hybrid materials. Materials used for obtaining drug-collagen hybrids were collagen type I (Coll) as matrix and fludarabine (F) and epirubicin (E) as hydrophilic active substances. After incorporation of drugs into Coll in differe...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.11.054

    authors: Voicu G,Geanaliu-Nicolae RE,Pîrvan AA,Andronescu E,Iordache F

    更新日期:2016-08-30 00:00:00

  • Dose tolerability of chronically inhaled voriconazole solution in rodents.

    abstract::Invasive pulmonary aspergillosis (IPA) is a fungal disease of the lung associated with high mortality rates in immunosuppressed patients despite treatment. Targeted drug delivery of aqueous voriconazole solutions has been shown in previous studies to produce high tissue and plasma drug concentrations as well as improv...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2009.06.003

    authors: Tolman JA,Nelson NA,Bosselmann S,Peters JI,Coalson JJ,Wiederhold NP,Williams RO 3rd

    更新日期:2009-09-08 00:00:00

  • Application of slurry bridging experiments at controlled water activities to predict the solid-state conversion between anhydrous and hydrated forms using theophylline as a model drug.

    abstract::The role of water activity (a(w)), relative humidity (RH) and temperature on the hydration state of theophylline has been investigated. Slurry bridging experiments at controlled water activities, using powder X-ray diffraction (PXRD) and thermogravimetric analysis (TGA) to characterise the solid phase, established tha...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00277-6

    authors: Ticehurst MD,Storey RA,Watt C

    更新日期:2002-10-24 00:00:00

  • Intranasal spray formulation containing rizatriptan benzoate for the treatment of migraine.

    abstract::Rizatriptan produces antimigraine activity by acting as selective agonist of 5-HT1B and 5-HT1D receptors present on intracranial and extracerebral blood vessels. Absorption from oral tablet is slow with Tmax of approximately 1-1.5 h. A few attempts have been made to promote rapid absorption such as oral or sublingual ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.118702

    authors: Chokshi A,Vaishya R,Inavolu R,Potta T

    更新日期:2019-11-25 00:00:00

  • Therapeutic efficacy of sustained drug release from chitosan gel on local inflammation.

    abstract::The model anti-inflammatory drug prednisolone (PS) was retained in chitosan (CS) gel beads, which were prepared in a 10% aqueous amino acid solution (pH 9.0). Sustained release of PS from the CS gel beads was observed. Carrageenan solution was injected into air pouches (AP), which were prepared subcutaneously on the d...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2003.11.036

    authors: Kofuji K,Akamine H,Qian CJ,Watanabe K,Togan Y,Nishimura M,Sugiyama I,Murata Y,Kawashima S

    更新日期:2004-03-19 00:00:00

  • Evaluation of the potential of ion pair formation to improve the oral absorption of two potent antiviral compounds, AMD3100 and PMPA.

    abstract::9-(2-phosphonyomethoxypropyl)adenine (PMPA) and AMD3100 are highly potent and selective antiretroviral agents. Since PMPA is negatively charged and AMD3100 positively charged at physiological pH, their transepithelial transport and their potential for oral drug delivery is very low. In this study, ion pair formation w...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00150-7

    authors: Van Gelder J,Witvrouw M,Pannecouque C,Henson G,Bridger G,Naesens L,De Clercq E,Annaert P,Shafiee M,Van den Mooter G,Kinget R,Augustijns P

    更新日期:1999-09-20 00:00:00

  • Investigation of 3D ordered macroporous carbon with different polymer coatings and their application as an oral vaccine carrier.

    abstract::3-D ordered macroporous carbon with different polymer coatings were developed as new oral vaccine immunological systems. Poly dimethyl diallyl ammonium (PDDA), polyethyleneimine (PEI) and chitosan (CTS), three different polymers with electropositive or adsorption-promoting properties, were chosen as the coating materi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.04.045

    authors: Zhao Q,Zhang Q,Yue Y,Huang J,Di D,Gao Y,Shao X,Wang S

    更新日期:2015-06-20 00:00:00

  • Development of a new method to characterize (SMBV) antigen formulations using surface plasmon resonance technology.

    abstract::Supra Molecular Biovectors (SMBV) are nanoparticles composed by a polysaccharidic core surrounded by a lipid bilayer. They are designed for drug delivery and vaccine and can be administrated by nasal route. The association rate and the stability of association between active principle (AP) or antigens (Ag) with SMBV c...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00227-2

    authors: Siguier JP,Major M,Balland O

    更新日期:2002-08-21 00:00:00

  • Effect of structural factors on release profiles of camptothecin from block copolymer conjugates with high load of drug.

    abstract::The aim of the present work was the synthesis and study the kinetics and profiles of camptothecin (CPT) release form block co- and ter-polymer conjugates comprising polylactide (PLA) segments and CPT moieties, structurally diverse by degrees of branching, content of d-PLA units and poly(ethylene glycol) methyl ether m...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.01.022

    authors: Plichta A,Kowalczyk S,Olędzka E,Sobczak M,Strawski M

    更新日期:2018-03-01 00:00:00

  • Detection and characterization of protein aggregates by fluorescence microscopy.

    abstract::Aggregation may compromise the stability as well as the biological activity of protein drugs. Detection of protein aggregates is needed in the process of protein characterization and during optimization of pharmaceutical formulations. This paper describes a technique, which consists of analysing protein aggregates by ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.08.024

    authors: Demeule B,Gurny R,Arvinte T

    更新日期:2007-02-01 00:00:00

  • Roll compaction process modeling: transfer between equipment and impact of process parameters.

    abstract::In this study, the roll compaction of an intermediate drug load formulation was performed using horizontally and vertically force fed roll compactors. The horizontally fed roll compactor was equipped with an instrumented roll technology allowing the direct measurement of normal stress at the roll surface, while the ve...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.02.042

    authors: Souihi N,Reynolds G,Tajarobi P,Wikström H,Haeffler G,Josefson M,Trygg J

    更新日期:2015-04-30 00:00:00

  • Production and evaluation of size reduced grades of microcrystalline cellulose.

    abstract::Size reduction of microcrystalline cellulose (MCC, Avicel PH-101) powder by ball milling was poorly effective, particularly in the presence of sodium lauryl sulphate (SLS), which tended to form a protective foam. Ultrasonic homogenisation of an aqueous suspension more readily produced ultra-fine MCC, even in the prese...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(00)00652-9

    authors: Levis SR,Deasy PB

    更新日期:2001-02-01 00:00:00

  • Characterization of nifedipine solid dispersions.

    abstract::The sublingual administration of nifedipine (NIF) is currently used in clinical practice. The sublingual administration of NIF solid dispersions (SD), by using a suitable dispenser, appears an interesting approach in the treatment of moderate and severe hypertensive emergencies. With this aim nine SD made of NIF and a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00173-4

    authors: Cilurzo F,Minghetti P,Casiraghi A,Montanari L

    更新日期:2002-08-21 00:00:00

  • Formation mechanism of colloidal nanoparticles obtained from probucol/PVP/SDS ternary ground mixture.

    abstract::The purpose of this study was to investigate the formation mechanism of colloidal nanoparticles after dispersion of probucol/polyvinylpyrrolidone (PVP)/sodium dodecyl sulphate (SDS) ternary ground mixture (GM) into water. Probucol, PVP and SDS were mixed at a weight ratio of 1:3:1 and ground for 30 min with a vibratio...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.10.052

    authors: Pongpeerapat A,Wanawongthai C,Tozuka Y,Moribe K,Yamamoto K

    更新日期:2008-03-20 00:00:00

  • Lubrication properties of potential alternative lubricants, glycerin fatty acid esters, to magnesium stearate.

    abstract::To study the usefulness of glycerin fatty acid ester Poem TR-FB (TR-FB) and Poem TR-HB (TR-HB) as lubricants, pressure transmission ratio, ejection force, disintegration time, and tensile strength were measured at different concentrations and mixing times for granules and tablets. When each lubricant was mixed at 0.1-...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2009.11.001

    authors: Uchimoto T,Iwao Y,Ikegami Y,Murata T,Sonobe T,Miyagishima A,Itai S

    更新日期:2010-02-15 00:00:00

  • Improved pH-dependent drug release and oral exposure of telmisartan, a poorly soluble drug through the formation of drug-aminoclay complex.

    abstract::Telmisartan (TEL) belongs to BCS class II (low solubility/high permeability) and exhibits the pH-dependent drug release. Since 3-aminopropyl functionalized magnesium phyllosilicate (aminoclay) can intercalate or adsorb the negatively charged molecules via the electrostatic interaction, TEL-aminoclay complex was synthe...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.05.009

    authors: Yang L,Shao Y,Han HK

    更新日期:2014-08-25 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

  • A systematic review of the use of dosage form manipulation to obtain required doses to inform use of manipulation in paediatric practice.

    abstract::This study sought to determine whether there is an evidence base for drug manipulation to obtain the required dose, a common feature of paediatric clinical practice. A systematic review of the data sources, PubMed, EMBASE, CINAHL, IPA and the Cochrane database of systematic reviews, was used. Studies that considered t...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2016.12.032

    authors: Richey RH,Hughes C,Craig JV,Shah UU,Ford JL,Barker CE,Peak M,Nunn AJ,Turner MA

    更新日期:2017-02-25 00:00:00

  • Solid dispersion of acetaminophen and poly(ethylene oxide) prepared by hot-melt mixing.

    abstract::In this study, a model drug, acetaminophen (APAP), was melt mixed with poly(ethylene oxide) (PEO) using a Brabender mixer. APAP was found to recrystallize upon cooling to room temperature for all the drug loadings investigated. Higher drug loading leads to faster recrystallization rate. However, the morphology of the ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.04.033

    authors: Yang M,Wang P,Huang CY,Ku MS,Liu H,Gogos C

    更新日期:2010-08-16 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

  • Enhanced solubility and modified release of poorly water-soluble drugs via self-assembled gelatin-oleic acid nanoparticles.

    abstract::Recently, we synthesized novel amphiphilic gelatin-oleic acid (GO) conjugate to prepare self-assembled nanoparticles for drug delivery. The aim of this study was to investigate pharmaceutical potentialities of self-assembled GO nanoparticles for solubility enhancement and modified release of poorly water-soluble drugs...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.07.025

    authors: Tran PH,Tran TT,Lee BJ

    更新日期:2013-10-15 00:00:00

  • Efficient gene delivery to primary human retinal pigment epithelial cells: The innate and acquired properties of vectors.

    abstract::The purpose of this study is designing non-viral gene delivery vectors for transfection of the primary human retinal pigment epithelial cells (RPE). In the design process of gene delivery vectors, considering physicochemical properties of vectors alone does not seem to be enough since they interact with constituents o...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.12.048

    authors: Tasharrofi N,Kouhkan F,Soleimani M,Soheili ZS,Atyabi F,Akbari Javar H,Abedin Dorkoosh F

    更新日期:2017-02-25 00:00:00

  • 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

  • Application of acid-treated yeast cell wall (AYC) as a pharmaceutical additive. III. AYC aqueous coating onto granules and film formation mechanism of AYC.

    abstract::From the viewpoint of effective utilization of natural resources and development of new pharmaceutical materials, acid-treated yeast cell wall (AYC) was prepared via a novel approach involving acidification of brewers' yeast cell wall. AYC aqueous dispersion containing 5% (w/v) AYC and 0.5% (w/v) glycerol was prepared...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00008-x

    authors: Yuasa H,Kaneshige J,Ozeki T,Kasai T,Eguchi T,Ishiwaki N

    更新日期:2002-04-26 00:00:00

  • A fast and reliable DSC-based method to determine the monomolecular loading capacity of drugs with good glass-forming ability in mesoporous silica.

    abstract::The aim of this study was to introduce a fast and reliable differential scanning calorimetry (DSC)-based method to determine the monomolecular loading capacity of drugs with good glass-forming ability in mesoporous silica (MS). The proposed method is based on a solvent-free melting/fusion of drug into the MS during a ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.04.035

    authors: Hempel NJ,Brede K,Olesen NE,Genina N,Knopp MM,Löbmann K

    更新日期:2018-06-10 00:00:00

  • Determination of acetaminophen's solubility in poly(ethylene oxide) by rheological, thermal and microscopic methods.

    abstract::A drug's solubility in a polymeric excipient is an important parameter that dictates the process window of hot-melt extrusion (HME) and product stability during storage. However, it is rather challenging to experimentally determine the solubility and there is very few published work in this field. In this study, the s...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.10.026

    authors: Yang M,Wang P,Suwardie H,Gogos C

    更新日期:2011-01-17 00:00:00