In vitro and in vivo characterization of nanoparticles made of MeO-PEG amine/PLA block copolymer and PLA.

Abstract:

:The preparative method of a block copolymer of poly(dl-lactic acid) (PLA) and methoxypolyethylene glycol amine (MeO-PEG(N)), named PLA-(MeO-PEG), was refined. The degree of introduction of MeO-PEG(N) into PLA increased up to 55% (mol/mol) using a dichloromethane/methanol mixture (1:1, v/v) as a solvent at the reductive amination and taking all the fractions of the first peak in gel-chromatography. Plain and 1,1'-Dioctadecyl-3,3,3',3'-tetramethylindodicarbocyanine (DiD)-loaded nanoparticles prepared using the PLA/PLA-(MeO-PEG) mixture of 45:55 (mol/mol) showed a mean size of 113 and 154 nm, respectively, and a positive zeta potential in water. DiD solution, i.v. administered, showed a lower plasma level and high distribution in liver, though DiD was distributed into the blood cells to a fair extent. Nanoparticles exhibited a higher plasma concentration of DiD than the DiD solution at 1 and 8h, though DiD was distributed into the liver and spleen to a fair extent. Nanoparticles made of the PLA/PLA-(MeO-PEG) mixture of 44:55 (mol/mol) showed better plasma retention than those made of the PLA/PLA-(MeO-PEG) mixture of 64:36 (mol/mol). It is suggested that the PLA/PLA-(MeO-PEG) mixture nanoparticles with a higher PEG/PLA ratio should be useful as a carrier for the elevation of the plasma concentration of lipophilic drugs.

journal_name

Int J Pharm

authors

Sasatsu M,Onishi H,Machida Y

doi

10.1016/j.ijpharm.2006.02.057

subject

Has Abstract

pub_date

2006-07-24 00:00:00

pages

167-74

issue

2

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(06)00217-1

journal_volume

317

pub_type

杂志文章
  • Development and characterisation of novel poly (vinyl alcohol)/poly (vinyl pyrrolidone)-based hydrogel-forming microneedle arrays for enhanced and sustained transdermal delivery of methotrexate.

    abstract::Methotrexate (MTX) is one of the mainstays of treatment for rheumatoid arthritis (RA) and juvenile idiopathic arthritis (JIA) and it is mainly administered either orally or by subcutaneous (SC) injection, which are not so satisfactory. While orally administered MTX is associated with variable bioavailability and cause...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119580

    authors: Tekko IA,Chen G,Domínguez-Robles J,Thakur RRS,Hamdan IMN,Vora L,Larrañeta E,McElnay JC,McCarthy HO,Rooney M,Donnelly RF

    更新日期:2020-08-30 00:00:00

  • In vitro and in silico characterization of fibrous scaffolds comprising alternate colistin sulfate-loaded and heat-treated polyvinyl alcohol nanofibrous sheets.

    abstract::A multilayer mat for dispensing colistin sulfate through a body surface was prepared by electrospinning. The fabricated system comprised various polyvinyl alcohol fibrous layers prepared with or without the active ingredient. One of the electrospun layers contained water-soluble colistin sulfate and the other was prep...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.03.044

    authors: Sebe I,Ostorházi E,Bodai Z,Eke Z,Szakács J,Kovács NK,Zelkó R

    更新日期:2017-05-15 00:00:00

  • Encapsulation of an antivasospastic drug, fasudil, into liposomes, and in vitro stability of the fasudil-loaded liposomes.

    abstract::The objectives of this work were to develop a liposomal fasudil, an antivasospastic drug, as a possible means to deliver the encapsulated drug to the brain, and to characterize the stability of the liposomal formulation in vitro. Transmembrane electrochemical gradients of H+ or ammonium sulfate were created, and their...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(01)00896-1

    authors: Ishida T,Takanashi Y,Doi H,Yamamoto I,Kiwada H

    更新日期:2002-01-31 00:00:00

  • Optimizing surfactant content to improve oral bioavailability of ibuprofen in microemulsions: just enough or more than enough?

    abstract::Microemulsions show excellent potential as drug delivery systems, but the surfactants used to prepare them can cause side effects. Researchers have explored various strategies to expand microemulsion area and thereby reduce the surfactant content necessary, but how these strategies affect drug oral bioavailability has...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.05.031

    authors: You X,Xing Q,Tuo J,Song W,Zeng Y,Hu H

    更新日期:2014-08-25 00:00:00

  • Evaluation of childhood exposure to di(2-ethylhexyl) phthalate from perfusion kits during long-term parenteral nutrition.

    abstract::Leachability of the plasticizer di(2-ethylhexyl) phthalate (DEHP) from administration sets into intravenous parenteral emulsions containing fat was investigated. DEHP is added to polyvinyl chloride (PVC) to impart flexibility. However, DEHP is a lipid-soluble suspected carcinogen that is hepatotoxic and teratogenic in...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(03)00335-1

    authors: Kambia K,Dine T,Gressier B,Bah S,Germe AF,Luyckx M,Brunet C,Michaud L,Gottrand F

    更新日期:2003-08-27 00:00:00

  • Supramolecular hydrogels as a universal scaffold for stepwise delivering Dox and Dox/cisplatin loaded block copolymer micelles.

    abstract::A general and simple method was presented for preparing supramolecular hydrogels to deliver anticancer drugs. In this system, hydrophobic anticancer drug doxorubicin (Dox) was loaded into poly(ethylene glycol)-b-poly(ε-caprolactone) (PEG-b-PCL) amphiphilic block copolymer micelles by hydrophobic interaction. The drug ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.08.007

    authors: Zhu W,Li Y,Liu L,Chen Y,Xi F

    更新日期:2012-11-01 00:00:00

  • Enzymatic action of phospholipase A₂ on liposomal drug delivery systems.

    abstract::The overexpression of secretory phospholipase A2 (sPLA2) in tumors has opened new avenues for enzyme-triggered active unloading of liposomal antitumor drug carriers selectively at the target tumor. However, the effects of the liposome composition, drug encapsulation, and tumor microenvironment on the activity of sPLA2...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.06.005

    authors: Hansen AH,Mouritsen OG,Arouri A

    更新日期:2015-08-01 00:00:00

  • Developability assessment of clinical drug products with maximum absorbable doses.

    abstract::Maximum absorbable dose refers to the maximum amount of an orally administered drug that can be absorbed in the gastrointestinal tract. Maximum absorbable dose, or D(abs), has proved to be an important parameter for quantifying the absorption potential of drug candidates. The purpose of this work is to validate the us...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.02.003

    authors: Ding X,Rose JP,Van Gelder J

    更新日期:2012-05-10 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

  • Permeation of cyproterone acetate through pig skin from different vehicles with phospholipids.

    abstract::The permeation of cyproterone acetate (CPA) from Derma Membrane Structure (DMS) creams and liposomal formulations was investigated. Standard diffusion experiments with dermatomed porcine skin were performed. The cumulative CPA amount permeated of the DMS creams was between 2.9 and 6.8 microg/cm(2) within 48 h. By addi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(03)00180-7

    authors: Valenta C,Janisch M

    更新日期:2003-06-04 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

  • Suppression of agglomeration in fluidized bed coating. II. Measurement of mist size in a fluidized bed chamber and effect of sodium chloride addition on mist size.

    abstract::It has been reported that the degree of particle agglomeration in fluidized bed coating is greatly affected by the spray mist size of coating solution. However, the mist size has generally been measured in open air, and few reports have described the measurement of the mist size in a chamber of the fluidized bed, in w...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(98)00370-6

    authors: Yuasa H,Nakano T,Kanaya Y

    更新日期:1999-02-01 00:00:00

  • Tumor selectivity of stealth multi-functionalized superparamagnetic iron oxide nanoparticles.

    abstract::Superparamagnetic iron oxide nanoparticles (SPIO-NPs) have traditionally been used as MRI contrast agent for disease imaging via passive targeting. However, there has been an increasing interest in the development of SPIO-NPs to cellular-specific targeting for imaging and drug delivery currently. The objective of our ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.10.038

    authors: Fan C,Gao W,Chen Z,Fan H,Li M,Deng F,Chen Z

    更新日期:2011-02-14 00:00:00

  • Anticancer effect of X-Ray triggered methotrexate conjugated albumin coated bismuth sulfide nanoparticles on SW480 colon cancer cell line.

    abstract::The application of nanoparticles (NPs) as radio-sensitizers and carriers has opened up a new horizon to overcome the limitations of chemo and radiotherapy. In this study, bovine serum albumin-coated Bi2S3 NPs (Bi2S3@BSA NPs) were synthesized and evaluated in terms of their ability to be used as a radio-sensitizer and ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119320

    authors: Faghfoori MH,Nosrati H,Rezaeejam H,Charmi J,Kaboli S,Johari B,Danafar H

    更新日期:2020-05-30 00:00:00

  • Influence of niacinamide containing formulations on the molecular and biophysical properties of the stratum corneum.

    abstract::Niacinamide-containing moisturisers are known be efficacious in alleviating dry skin conditions and improving stratum corneum (SC) barrier function. However, the mechanisms of action of niacinamide at the molecular level in the SC are still not well understood. Previously, we have reported the development of novel met...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,随机对照试验

    doi:10.1016/j.ijpharm.2012.11.043

    authors: Mohammed D,Crowther JM,Matts PJ,Hadgraft J,Lane ME

    更新日期:2013-01-30 00:00:00

  • Plasma pharmacokinetics and distribution of ruxolitinib into skin following oral and topical administration in minipigs.

    abstract::This preclinical study compared plasma concentrations and distribution of ruxolitinib in the skin of Göttingen minipigs following twice a day oral (40 mg/kg) versus topical administration (1.5% w/w cream applied to 10% of body surface area). Following oral administration, the plasma area-under-the-curve was approximat...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119889

    authors: Persaud I,Diamond S,Pan R,Burke K,Harris J,Conlin M,Yeleswaram S

    更新日期:2020-11-30 00:00:00

  • Direct compression properties of melt-extruded isomalt.

    abstract::Isomalt, a sugar alcohol, was melt-extruded prior to compression in order to improve its tabletting properties. After fusion, crystalline isomalt was transformed into an amorphous form as shown by X-ray diffraction and differential scanning calorimetry (DSC). The tabletting properties of amorphous isomalt were dramati...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(01)00993-0

    authors: Ndindayino F,Henrist D,Kiekens F,Van den Mooter G,Vervaet C,Remon JP

    更新日期:2002-03-20 00:00:00

  • Lectin-coated PLGA microparticles: thermoresponsive release and in vitro evidence for enhanced cell interaction.

    abstract::PLGA-microparticles with 4.7 μm in diameter were prepared by the double emulsion technique and loaded with 1.7 μg fluorescein/mg PLGA mimicking a hydrophilic API. In an effort to further elucidate the release and bioadhesive characteristics of lectin-grafted formulations in vitro, the particles were coated with wheat ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.07.025

    authors: Wang XY,Koller R,Wirth M,Gabor F

    更新日期:2012-10-15 00:00:00

  • Formation of multicellular tumor spheroids induced by cyclic RGD-peptides and use for anticancer drug testing in vitro.

    abstract::Development of novel anticancer formulations is a priority challenge in biomedicine. However, in vitro models based on monolayer cultures (2D) which are currently used for cytotoxicity tests leave much to be desired. More and more attention is focusing on 3D in vitro systems which can better mimic solid tumors. The ai...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.04.005

    authors: Akasov R,Zaytseva-Zotova D,Burov S,Leko M,Dontenwill M,Chiper M,Vandamme T,Markvicheva E

    更新日期:2016-06-15 00:00:00

  • Effect of granule properties on rough mouth feel and palatability of orally disintegrating tablets.

    abstract::In this study, we evaluated the palatability of orally disintegrating tablets (ODTs) containing core granules with different particle sizes, coating, and types of materials using visual analog scales (VAS). Tableting the core granules into ODTs reduced rough mouth feel and improved overall palatability compared to the...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,随机对照试验

    doi:10.1016/j.ijpharm.2015.02.023

    authors: Kimura S,Uchida S,Kanada K,Namiki N

    更新日期:2015-04-30 00:00:00

  • Improvement of absorption enhancing effects of n-dodecyl-beta-D-maltopyranoside by its colon-specific delivery using chitosan capsules.

    abstract::In general, absorption enhancing effects of various absorption enhancers were greater in the large intestine than those in the small intestinal regions. Therefore, the effectiveness of absorption enhancers is expected to be remarkably observed, if these enhancers can be delivered to the large intestine with some poorl...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.12.017

    authors: Fetih G,Lindberg S,Itoh K,Okada N,Fujita T,Habib F,Artersson P,Attia M,Yamamoto A

    更新日期:2005-04-11 00:00:00

  • Evaluating particle hardness of pharmaceutical solids using AFM nanoindentation.

    abstract::Understanding mechanical properties of pharmaceutical solids at the submicron scale can be very important to pharmaceutical research & development. In this paper, the hardness of individual particles of various pharmaceutical solids including sucrose, lactose, ascorbic acid, and ibuprofen was quantified using the atom...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.06.015

    authors: Masterson VM,Cao X

    更新日期:2008-10-01 00:00:00

  • Single-ligand dual-targeting irinotecan liposomes: Control of targeting ligand display by pH-responsive PEG-shedding strategy to enhance tumor-specific therapy and attenuate toxicity.

    abstract::Along with the malignant proliferation of tumor requiring nutrients, the expression of L-type amino acid transporter 1(LAT1) and amino acid transporter B0,+ (ATB0,+) in cancer cells is up-regulated that can be used as new targets for active targeting of tumor. However, since normal cells also express amino acid transp...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119680

    authors: Wang Z,Lin X,Chi D,Xu Z,Lin G,Liu H,Sun J,He Z,Wang Y

    更新日期:2020-09-25 00:00:00

  • Microemulsions containing long-chain oil ethyl oleate improve the oral bioavailability of piroxicam by increasing drug solubility and lymphatic transportation simultaneously.

    abstract::Drug solubility and lymphatic transport enhancements are two main pathways to improve drug oral bioavailability for microemulsions. However, it is not easy to have both achieved simultaneously because excipients used for improving lymphatic transport were usually insufficient in forming microemulsions and solubilizing...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.07.061

    authors: Xing Q,Song J,You X,Xu D,Wang K,Song J,Guo Q,Li P,Wu C,Hu H

    更新日期:2016-09-25 00:00:00

  • Development of artemether-loaded nanostructured lipid carrier (NLC) formulation for topical application.

    abstract::NLC topical formulation as an alternative to oral and parenteral (IM) delivery of artemether (ART), a poorly water-soluble drug was designed. A Phospholipon 85G-modified Gelucire 43/01 based NLC formulation containing 75% Transcutol was chosen from DSC studies and loaded with gradient concentration of ART (100-750 mg)...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.10.004

    authors: Nnamani PO,Hansen S,Windbergs M,Lehr CM

    更新日期:2014-12-30 00:00:00

  • Influence of membrane structure on the preparation of colloidal lipid dispersions by premix membrane emulsification.

    abstract::Since premix membrane emulsification was developed as alternative technique for the preparation of emulsions and solid lipid particles as carrier systems for lipophilic drugs, many types of membranes have been used in this preparation process. The purpose of this study was to evaluate the influence of different types ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.02.013

    authors: Joseph S,Bunjes H

    更新日期:2013-03-25 00:00:00

  • Paclitaxel isomerisation in polymeric micelles based on hydrophobized hyaluronic acid.

    abstract::Physical and chemical structure of paclitaxel (PTX) was studied after its incorporation into polymeric micelles made of hyaluronic acid (HA) (Mw=15 kDa) grafted with C6 or C18:1 acyl chains. PTX was physically incorporated into the micellar core by solvent evaporation technique. Maximum loading capacity for HAC6 and H...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.03.024

    authors: Smejkalová D,Nešporová K,Hermannová M,Huerta-Angeles G,Cožíková D,Vištejnová L,Safránková B,Novotný J,Kučerík J,Velebný V

    更新日期:2014-05-15 00:00:00

  • Arsenic release from glass containers by action of intravenous nutrition formulation constituents.

    abstract::Pharmacopoeias prescribe tests to determine the levels of arsenic in raw materials and glass containers. In this study, glass ampoules for injectables containing individually the main components of intravenous nutrition formulations were submitted to the hydrolytic resistance test by heating at 121 degrees C for 30 mi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.02.008

    authors: Bohrer D,Becker E,Nascimento PC,Mörschbächer V,de Carvalho LM,da Silva Marques M

    更新日期:2006-06-06 00:00:00

  • In vitro and in vivo correlation of disintegration and bitter taste masking using orally disintegrating tablet containing ion exchange resin-drug complex.

    abstract::Although the taste-masking of bitter drug using ion exchange resin has been recognized, in vitro testing using an electronic tongue (e-Tongue) and in vivo bitterness test by human panel test was not fully understood. In case of orally disintegrating tablet (ODT) containing bitter medicine, in vitro and in vivo disinte...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.07.072

    authors: Kim JI,Cho SM,Cui JH,Cao QR,Oh E,Lee BJ

    更新日期:2013-10-15 00:00:00

  • Gastro-floating tablets of cephalexin: preparation and in vitro/in vivo evaluation.

    abstract::Gastro-floating tablets of cephalexin were developed to prolong the residence time in major absorption sites. Gastro-floating tablets were prepared and optimized using hydroxypropyl methylcellulose (HPMC K100M) as matrix and sodium bicarbonate as a gas-forming agent. The properties of the tablets in terms of floating ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.05.011

    authors: Yin L,Qin C,Chen K,Zhu C,Cao H,Zhou J,He W,Zhang Q

    更新日期:2013-08-16 00:00:00