Delivery of FK506-loaded PLGA nanoparticles prolongs cardiac allograft survival.

Abstract:

:In this study, FK506-loaded poly(lactide-co-glycolide) nanoparticles (PLGA-FK506-NPs) were developed using an O/W emulsion solvent evaporation method. The PLGA-FK506-NPs were observed to be monodispersed and spherical by transmission and scanning electron microscopy. The mean size and zeta potential measured by dynamic light scattering were 110 ± 1.3 nm and -20.56 ± 3.65 mV, respectively. The FK506 entrapment and loading efficiency were 94.46 ± 1.88% and 5.38 ± 0.24%, respectively. Moreover, a pharmacokinetics study revealed that the PLGA-FK506-NPs behaved significantly different than free FK506 by exhibiting a higher area under curve (1.69-fold), higher mean residence time (1.29-fold), slower clearance and longer elimination half-life. Notably, the concentrations of FK506 in the spleen and mesenteric lymph nodes of the PLGA-FK506-NP group were 3.1-fold and 2.9-fold higher than those of the free FK506 group. Furthermore, the immunosuppressive efficacy was evaluated in a rat heterotopic heart transplantation model, and the results showed that PLGA-FK506-NP treatment could successfully alleviate acute rejection and prolong allograft survival compared with the free FK506 treatment (mean survival time, 17.1 ± 2.0 versus 13.3 ± 1.7 days). In conclusion, PLGA-FK506-NPs are a promising formulation for spleen and lymph node delivery and have potential use in the treatment of cardiac allograft acute rejection.

journal_name

Int J Pharm

authors

Deng C,Chen Y,Zhang L,Wu Y,Li H,Wu Y,Wang B,Sun Z,Li Y,Lv Q,Yang Y,Wang J,Jin Q,Xie M

doi

10.1016/j.ijpharm.2019.118951

subject

Has Abstract

pub_date

2020-02-15 00:00:00

pages

118951

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(19)30996-2

journal_volume

575

pub_type

杂志文章
  • Characterization of alginate/poly-L-lysine particles as antisense oligonucleotide carriers.

    abstract::The gel forming characteristics of alginate in the presence of calcium ions and further crosslinking with poly-L-lysine led to the formation of sponge-like nano- and microparticles. The particle size was varied by adjusting the final concentrations of and proportions between the components. The region for particle for...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00030-3

    authors: González Ferreiro M,Tillman L,Hardee G,Bodmeier R

    更新日期:2002-06-04 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

  • 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

  • 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

  • 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

  • Mechanistic study on rapid fabrication of fibrous films via centrifugal melt spinning.

    abstract::Fibrous films have attracted considerable attention in the field of drug delivery and wound dressings owing to their porous structure and highly aligned fiber orientation. However, current fabrication methods such as electrospinning have certain limitations, including high voltage requirement and conductivity dependen...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.02.005

    authors: Yang Y,Zheng N,Zhou Y,Shan W,Shen J

    更新日期:2019-04-05 00:00:00

  • A biocompatible and easy-to-make polyelectrolyte dressing with tunable drug delivery properties for wound care.

    abstract::Chitosan (CS) is a biodegradable and biocompatible polysaccharide which displays immune-stimulatory effects and anti-bacterial properties to facilitate wound closure. Over the years, different CS-based dressings have been developed; however, most of them are not fully biodegradable due to the involvement of synthetic ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.05.045

    authors: Lai WF,Hu C,Deng G,Lui KH,Wang X,Tsoi TH,Wang S,Wong WT

    更新日期:2019-07-20 00:00:00

  • Sponges carrying self-microemulsifying drug delivery systems.

    abstract::Self-microemulsifying drug delivery systems (SMEDDS) increase the solubility of lipophilic drugs. One barrier to their wide application is their liquid nature. We report on a new method to solidify SMEDDS-their incorporation in sponges made from a hydrophilic natural polymer. Using different freeze-drying schemes, spo...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.09.024

    authors: Josef E,Bianco-Peled H

    更新日期:2013-12-15 00:00:00

  • Lipase degradation of Dynasan 114 and 116 solid lipid nanoparticles (SLN)--effect of surfactants, storage time and crystallinity.

    abstract::In vivo drug release from solid lipid nanoparticles (SLN) takes place by diffusion and degradation of the lipid matrix. SLN with different degree of crystallinity were prepared to study the effect of crystallinity on the degradation velocity. These SLN were produced by using glycerides with different length of fatty a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00035-2

    authors: Olbrich C,Kayser O,Müller RH

    更新日期:2002-04-26 00:00:00

  • Robustness testing, using experimental design, of a flow-through dissolution method for a product where the actives have markedly differing solubility properties.

    abstract::The use of experimental design for the robustness testing of a flow-through dissolution method (Ph Eur/USP Apparatus 4) for atovaquone, one of the drug substances in a dual-active anti-malarial tablet formulation, Malarone tablets, is described. This procedure was developed to overcome the suppression of the atovaquon...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(00)00509-3

    authors: Bloomfield MS,Butler WC

    更新日期:2000-09-25 00:00:00

  • Development of new polymer-based particulate systems for anti-glioma vaccination.

    abstract::Biodegradable and biocompatible microspheres represent a promising alternative to conventional adjuvants for anti-tumour vaccination. Focusing on glioma, we developed two poly(D,L-lactide-co-glycolide) (PLGA)-based particulate systems presenting tumour antigens associated with plasma membranes or with cell lysates. Gl...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.10.046

    authors: Sapin A,Garcion E,Clavreul A,Lagarce F,Benoit JP,Menei P

    更新日期:2006-02-17 00:00:00

  • Penetration of topical and oral ofloxacin into the aqueous and vitreous humor of inflamed rabbit eyes.

    abstract:PURPOSE:This study aimed to investigate the penetration of topical and oral ofloxacin into aqueous humor and vitreous humor in post-traumatic endophthalmitis model in rabbits. METHODS:A standardized intraocular infection after penetrating injury was made in the right eyes of 16 rabbits. Intraocular infection was induc...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(00)00482-8

    authors: Oztürk F,Kurt E,Inan UU,Kortunay MC,Ilker SS,Başci NE,Bozkurt A

    更新日期:2000-08-25 00:00:00

  • Evaluation of the vibratory feeder method for assessment of powder flow properties.

    abstract::The flow properties of pharmaceutical powders and blends used in solid oral dosage forms are an important consideration during dosage form development. The vibratory feeder method, a flow measurement technique that quantifies avalanche flow, has been adapted for measurement of the flow properties of common pharmaceuti...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2003.09.024

    authors: Bhattachar SN,Hedden DB,Olsofsky AM,Qu X,Hsieh WY,Canter KG

    更新日期:2004-01-28 00:00:00

  • Slow-release of famotidine from tablets consisting of chitosan/sulfobutyl ether β-cyclodextrin composites.

    abstract::An intermolecular complex formed from a 1:1 weight ratio of chitosan (CS, molecular weight 30 kDa) and sulfobutyl ether β-cyclodextrin (SBE-β-CyD, degree of substitution 7) was less soluble than either of the original components. The release of famotidine from tablets composed of a simple mixture of CS and SBE-β-CyD i...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.04.022

    authors: Anraku M,Hiraga A,Iohara D,Pipkin JD,Uekama K,Hirayama F

    更新日期:2015-06-20 00:00:00

  • In vitro release properties of etonogestrel and ethinyl estradiol from a contraceptive vaginal ring.

    abstract::The release properties of steroids from a combined contraceptive vaginal ring have been investigated. The product design is based on a coaxial fiber consisting of two types of polyethylene vinylacetate copolymers. Inside the core of the fiber, two steroids are present in a molecularly dissolved state. In order to desi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(01)00900-0

    authors: van Laarhoven JA,Kruft MA,Vromans H

    更新日期:2002-01-31 00:00:00

  • A novel administration route for edaravone: I. Effects of metabolic inhibitors on skin permeability of edaravone.

    abstract::We examined the effects of metabolic inhibitors on skin permeation of edaravone. SKF-525A, diclofenac sodium (DIC) and indomethacin (IND) were added to supernatant fluid (SF) of hairless rat (HR) skin homogenate. L-Cysteine (L-Cys) and benzotriazole (BTA), as pharmaceutical additives, were added to HR skin homogenate ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.12.038

    authors: Sato T,Mizuno K,Ishii F

    更新日期:2009-05-08 00:00:00

  • Effect of vehicles and penetration enhancers on the in vitro percutaneous absorption of tenoxicam through hairless mouse skin.

    abstract::The effects of vehicles and penetration enhancers on the in vitro permeation of tenoxicam from saturated solutions through dorsal hairless mouse skin were investigated. Various types of vehicles, including ester-, alcohol-, and ether-types and their mixtures, were used as vehicles, and then a series of fatty acids and...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00009-1

    authors: Gwak HS,Chun IK

    更新日期:2002-04-02 00:00:00

  • Transcutaneous immunisation assisted by low-frequency ultrasound.

    abstract::Low-frequency ultrasound application is known to increase the skin's permeability to large molecules such as vaccines, and to enable transcutaneous immunisation. Sodium dodecyl sulphate (SDS) - a skin irritant - is often included in the coupling medium at 1% (w/v), as this has been found to enhance skin permeability. ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.10.014

    authors: Dahlan A,Alpar HO,Stickings P,Sesardic D,Murdan S

    更新日期:2009-02-23 00:00:00

  • Investigation of in vitro PDT activities of zinc phthalocyanine immobilised TiO2 nanoparticles.

    abstract::Phthalocyanines (Pcs) are commonly used as Photosensors (PSs) in Photodynamic Therapy (PDT) applications due to their intense absorption in the far red-near IR spectral region with a high extinction coefficient and high ability for generating singlet oxygen. Pcs targetspecifically tumors, and do not show any considera...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.03.050

    authors: Yurt F,Ince M,Colak SG,Ocakoglu K,Er O,Soylu HM,Gunduz C,Avci CB,Kurt CC

    更新日期:2017-05-30 00:00:00

  • Ultrasonic real-time in-die monitoring of the tablet compaction process-a proof of concept study.

    abstract::The mechanical properties of a drug tablet can affect its performance (e.g., dissolution profile and its physical robustness. An ultrasonic system for real-time in-die tablet mechanical property monitoring during compaction has been demonstrated. The reported set-up is a proof of concept compaction monitoring system w...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.09.014

    authors: Stephens JD,Kowalczyk BR,Hancock BC,Kaul G,Cetinkaya C

    更新日期:2013-02-14 00:00:00

  • Novel O-palmitoylscleroglucan-coated liposomes as drug carriers: development, characterization and interaction with leuprolide.

    abstract::Polysaccharide-coated liposomes have been studied for their potential use for peptide drug delivery by the oral route because they are able to minimize the disruptive influences on peptide drugs of gastrointestinal fluids. The aim of this work was to synthesize and characterize a modified polysaccharide, O-palmitoylsc...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.06.040

    authors: Carafa M,Marianecci C,Annibaldi V,Di Stefano A,Sozio P,Santucci E

    更新日期:2006-11-15 00:00:00

  • Mechanical particle coating using ethylcellulose nanoparticle agglomerates for preparing controlled release fine particles; effect of coating temperature on coating performance.

    abstract::This study describes the effect of coating temperature on the performance of mechanical particle coating using ethylcellulose, which was done to produce controlled-release particles (diameters less than 100 μm) with different release rates. First, theophylline crystals were spheronized using a mechanical powder proces...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.11.061

    authors: Kondo K,Ando C,Niwa T

    更新日期:2019-01-10 00:00:00

  • Inorganic-polymer nanohybrid carrier for delivery of a poorly-soluble drug, ursodeoxycholic acid.

    abstract::Delivery of poorly soluble drugs has been problematic due to its low absorption profile and bioavailability. In this work, ursodeoxycholic acid (UDCA), a poorly-soluble drug, was intercalated into inorganic nanovehicle, layered double hydroxides (LDHs), with a molecular level to enhance its solubility in biological fl...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.09.039

    authors: Choi G,Lee JH,Oh YJ,Choy YB,Park MC,Chang HC,Choy JH

    更新日期:2010-12-15 00:00:00

  • Preparation and investigation of core-shell nanoparticles containing human interferon-α.

    abstract::Sustained release of active interferon-α (IFN-α) has been achieved from core-shell nanoparticles (NPs) prepared by aqueous precipitation of IFN-α-enriched human serum albumin (HSA-IFN-α) and layer-by-layer (L-b-L) by coating of the IFN-α NPs with poly(sodium-4-styrene) sulphonate (PSS) and chitosan (Chit). The concent...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.118825

    authors: Kristó K,Szekeres M,Makai Z,Márki Á,Kelemen A,Bali L,Pallai Z,Dékány I,Csóka I

    更新日期:2020-01-05 00:00:00

  • Dehydration of trehalose dihydrate at low relative humidity and ambient temperature.

    abstract::The physico-chemical behaviour of trehalose dihydrate during storage at low relative humidity and ambient temperature was investigated, using a combination of techniques commonly employed in pharmaceutical research. Weight loss, water content determinations, differential scanning calorimetry and X-ray powder diffracti...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.01.026

    authors: Jones MD,Hooton JC,Dawson ML,Ferrie AR,Price R

    更新日期:2006-04-26 00:00:00

  • Development of a cyclodextrin-based aqueous cyclosporin A eye drop formulations.

    abstract::Cyclosporin A (CyA) is a lipophilic, cyclic polypeptide drug with anti-inflammatory properties. It is used in topical treatment of dry eyes and is now commercially available in oil based surfactant containing eye drops. Surfactants can irritate the eye surface causing burning, itching and irritation of the conjunctiva...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.07.040

    authors: Jóhannsdóttir S,Jansook P,Stefánsson E,Loftsson T

    更新日期:2015-09-30 00:00:00

  • Biopharmaceutic evaluation of novel anthelmintic (1H-benzimidazol-5(6)-yl)carboxamide derivatives.

    abstract::Benzimidazole 2-carbamates, such as albendazole (ABZ) and mebendazole (MBZ), used for the treatment of helmintic infections, have low aqueous solubility and poor bioavailability, both of which lead to high interindividual variability when used for human systemic helmintiosis; therefore, it is necessary to search for n...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.05.013

    authors: Rivera JC,Yépez-Mulia L,Hernández-Campos A,Moreno-Esparza R,Castillo R,Navarrete-Vázquez G,Fuentes-Noriega I,Jung-Cook H

    更新日期:2007-10-01 00:00:00

  • Effect of preparation technique on the properties of liposomes encapsulating ketoprofen-cyclodextrin complexes aimed for transdermal delivery.

    abstract::The combined approach of cyclodextrin complexation and entrapment in liposomes was investigated in order to develop an effective topical formulation of ketoprofen. Equimolar complex of drug and hydroxypropyl-beta-cyclodextrin (HPbetaCyd) was added at different concentrations to the aqueous phase of liposomes consistin...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.12.047

    authors: Maestrelli F,González-Rodríguez ML,Rabasco AM,Mura P

    更新日期:2006-04-07 00:00:00

  • Characterisation of recombinant factor IX before and after GlycoPEGylation.

    abstract::The effect of the GlycoPEGylation process used for prolonging the half-life of recombinant factor IX (rFIX) has no impact on the primary and higher order structure of activated factor IX. Characterisation work performed on recombinant factor IX and on the GlycoPEGylated form of rFIX (N9-GP), confirm that the primary s...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119654

    authors: Nielsen FS,Schmidt AS,Kristensen AK,Nielsen AD,Kristensen BK,Palm L

    更新日期:2020-10-15 00:00:00

  • Kinetic stability studies of HBV vaccine in a microneedle patch.

    abstract::This study systematically demonstrated the antigenicity kinetics of HBV vaccine microneedles (MNs) during the fabrication, application and storage. To improve the stability of HBsAg in a microneedle patch, several selected saccharides were added to the MN formulations as stabilizers. According to the experimental data...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.118489

    authors: Zhu DD,Zhang XP,Yu HL,Liu RX,Shen CB,Zhang WF,Cui Y,Guo XD

    更新日期:2019-08-15 00:00:00