Phospholipid components of the synthetic pulmonary surfactant CHF5633 probed by fluorescence spectroscopy.

Abstract:

:CHF5633 (Chiesi Farmaceutici, Italy) is a synthetic pulmonary surfactant currently under clinical development for the treatment of Respiratory Distress Syndrome in premature infants. The product is composed of phospholipids in liposomal organization, together with two peptide analogues of human surfactant proteins B and C. Phospholipids in liposomes can undergo oxidation of unsaturated lipids and hydrolysis, with formation of fatty acids and lysolipids, both affecting the physico-chemical properties of the formulation. We exploited two fluorescence probes, Prodan and ADIFAB, to evaluate the stability of the phospholipid components of CHF5633. While Prodan enters the phospholipid bilayer and probes the polarity of this environment, ADIFAB binds free fatty acids in the aqueous phase, allowing to determine their concentration. Changes of Prodan fluorescence emission indicated an increase in the polarity of the phospholipid bilayer as a function of time. This behavior is coupled with an increase in fatty acids concentration in the aqueous phase, as determined by ADIFAB, and an increase in lysolipids concentration, as determined by HPLC-MS. Prodan and ADIFAB resulted efficient probes to monitor phospholipids hydrolysis in liposomes, reporting an increased stability of CHF5633 at pH values higher than 6.5.

journal_name

Int J Pharm

authors

Faggiano S,Ronda L,Raboni S,Sartor F,Cavatorta V,Sgarbi E,Caivano G,Pertile M,Mozzarelli A

doi

10.1016/j.ijpharm.2018.10.045

subject

Has Abstract

pub_date

2018-12-20 00:00:00

pages

290-297

issue

1-2

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(18)30783-X

journal_volume

553

pub_type

杂志文章
  • Pluripotent stem cells as new drugs? The example of Parkinson's disease.

    abstract::Cell replacement therapy is a widely discussed novel concept of medical treatment. The increased knowledge in the stem cell field, particularly pluripotent stem cells, potentially provides powerful tools for this therapeutic concept. A large number of disease characterized by the loss of functional cells are potential...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2009.03.003

    authors: Preynat-Seauve O,Burkhard PR,Villard J,Zingg W,Ginovart N,Feki A,Dubois-Dauphin M,Hurst SA,Mauron A,Jaconi M,Krause KH

    更新日期:2009-11-03 00:00:00

  • Targeted antifungal delivery system: beta-glucosidase sensitive nystatin-star poly(ethylene glycol) conjugate.

    abstract::A new targeted intravenous conjugate of nystatin with pentaerythritol poly(ethylene glycol)ether has been prepared and characterised (NY(4)-sPEG, M=25 160). The conjugate contains a beta-d-glucopyranoside molecular switch sensitive to beta-glucosidases (E.C.3.2.1.21), which are specifically present in the enzyme outfi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2009.10.034

    authors: Bílková E,Imramovský A,Buchta V,Sedlák M

    更新日期:2010-02-15 00:00:00

  • Process and formulation characterizations of the thermal adhesion granulation (TAG) process for improving granular properties.

    abstract::In this study, we demonstrate the feasibility of using the thermal adhesion granulation (TAG) method to improve granular properties for preparing highly compressible excipients as direct tabletting aids. The TAG method subjects a mixture containing excipients, such as microcrystalline cellulose (MCC), lactose, starch,...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.02.002

    authors: Lin HL,Ho HO,Chen CC,Yeh TS,Sheu MT

    更新日期:2008-06-05 00:00:00

  • Liposomes encapsulating native and cyclodextrin enclosed paclitaxel: Enhanced loading efficiency and its pharmacokinetic evaluation.

    abstract::Combination strategy involving cyclodextrin (CD) complexation and liposomal system was investigated for Paclitaxel (PTX) to improve loading. Complexation was done using 2,6-di-O-methylbetacyclodextrin (DMβCD). Sterically stabilized double loaded PEGylated liposomes (DLPLs) containing PTX and PTX-DMβCD complex were pre...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.11.048

    authors: Bhatt P,Lalani R,Vhora I,Patil S,Amrutiya J,Misra A,Mashru R

    更新日期:2018-01-30 00:00:00

  • Amino Acid-functionalized hollow mesoporous silica nanospheres as efficient biocompatible drug carriers for anticancer applications.

    abstract::Herein, a series of new amino acid-functionalized hollow mesoporous silica nanospheres (HMSNs) by post-grafting methods were prepared. These new materials were characterized by different techniques and were studied as matrices for the antineoplastic drug (cisplatin) transport and delivery. The results demonstrate that...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.118709

    authors: Ezzati N,Mahjoub AR,Abolhosseini Shahrnoy A,Syrgiannis Z

    更新日期:2019-12-15 00:00:00

  • Anticancer siRNA cocktails as a novel tool to treat cancer cells. Part (B). Efficiency of pharmacological action.

    abstract::This paper examines a perspective to use newly engineered nanomaterials as effective and safe carriers for gene therapy of cancer. Three different groups of cationic dendrimers (PAMAM, phosphorus, and carbosilane) were complexed with anticancer siRNA and the biophysical properties of the dendriplexes created were anal...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.03.034

    authors: Dzmitruk V,Szulc A,Shcharbin D,Janaszewska A,Shcharbina N,Lazniewska J,Novopashina D,Buyanova M,Ionov M,Klajnert-Maculewicz B,Gómez-Ramirez R,Mignani S,Majoral JP,Muñoz-Fernández MA,Bryszewska M

    更新日期:2015-05-15 00:00:00

  • In-vitro and particle image velocimetry studies of dry powder inhalers.

    abstract::Inhalation drug delivery has seen a swift rise in the use of dry powder inhalers (DPIs) to treat chronic respiratory conditions. However, universal adoption of DPIs has been restrained due to their low efficiencies and significant drug losses in the mouth-throat region. Aerosol efficiency of DPIs is closely related to...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119966

    authors: Dos Reis LG,Chaugule V,Fletcher DF,Young PM,Traini D,Soria J

    更新日期:2021-01-05 00:00:00

  • Characterization of a diltiazem-lambda carrageenan complex.

    abstract::In the present paper the interaction between lambda carrageenan, a natural sulphated polysaccharide, and diltiazem HCl, a Ca channel blocking agent, was studied. Dialysis equilibria were performed to quantify the binding capacity of lambda carrageenan for diltiazem. The relevance of the interaction to hydrophilic matr...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(00)00389-6

    authors: Bonferoni MC,Rossi S,Ferrari F,Bettinetti GP,Caramella C

    更新日期:2000-05-10 00:00:00

  • Oral bioavailability and hypoglycaemic activity of tolbutamide/cyclodextrin inclusion complexes.

    abstract::The purpose of the present study was to evaluate the enhancement of tolbutamide (TBM) oral bioavailability and hypoglycaemic activity through complexation with beta-cyclodextrin (beta-CD) and hydroxypropyl-beta-cyclodextrin (HP-beta-CD). TBM and its freeze-dried inclusion complexes were administered to rabbits (New ze...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(00)00445-2

    authors: Veiga F,Fernandes C,Teixeira F

    更新日期:2000-07-20 00:00:00

  • Nutlin-3 loaded nanocarriers: Preparation, characterization and in vitro antineoplastic effect against primary effusion lymphoma.

    abstract::In this investigation, Nutlin-3 (Nut3), a novel antitumor drug with low water solubility (<0.1mg/L at 25°C), was loaded into liposomes (Lipo-Nut3), polymeric nanoparticles (NPs-Nut3) and nanoparticles engineered with an antibody direct against Syndecan-1/CD 138 (Syn-NPs-Nut3) to obtain carriers targeted to PEL (primar...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.05.029

    authors: Belletti D,Tosi G,Riva G,Lagreca I,Galliania M,Luppi M,Vandelli MA,Forni F,Ruozi B

    更新日期:2015-07-25 00:00:00

  • Mucoadhesivity and release properties of quaternary ammonium-chitosan conjugates and their nanoparticulate supramolecular aggregates: an NMR investigation.

    abstract::Selective relaxation rate measurements effectively proved the affinity of dexamethasone 21-phosphate disodium salt for quaternary ammonium-chitosan conjugates, their thiolated derivatives and the corresponding nanostructured aggregates. Affinity was also probed by dynamic dialysis. The release profile of dexamethasone...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.12.018

    authors: Uccello-Barretta G,Balzano F,Aiello F,Senatore A,Fabiano A,Zambito Y

    更新日期:2014-01-30 00:00:00

  • Near-infrared spectroscopy (NIRS) and chemometric analysis of Malaysian and UK paracetamol tablets: a spectral database study.

    abstract::The influx of medicines from different sources into healthcare systems of developing countries presents a challenge to monitor their origin and quality. The absence of a repository of reference samples or spectra prevents the analysis of tablets by direct comparison. A set of paracetamol tablets purchased in Malaysian...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.05.057

    authors: Said MM,Gibbons S,Moffat AC,Zloh M

    更新日期:2011-08-30 00:00:00

  • Paediatric formulations--getting to the heart of the problem.

    abstract::Many medicines prescribed for children are unlicensed. Solid dosage forms present problems as children have difficulty swallowing whole tablets or capsules. When medicines are not licensed for children, it is unlikely that there will be a suitable, licensed liquid formulation and so extemporaneous liquid preparations ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.05.006

    authors: Standing JF,Tuleu C

    更新日期:2005-08-26 00:00:00

  • Synthesis and characterization of hydrogels formed from a glycidyl methacrylate derivative of galactomannan.

    abstract::The present investigation describes a procedure for the synthesis of a glycidyl methacrylated derivative from galactomannan, GA-MA, and the respective hydrogel formation. The galactomannan (GA), raw material, was purified and dissolved in DMSO. After dissolution, 4-dimethyl-amino-pyridine (DMAP) and glycidyl methacryl...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2003.08.001

    authors: Reis AV,Cavalcanti OA,Rubira AF,Muniz EC

    更新日期:2003-11-28 00:00:00

  • Enhanced anti-glioblastoma efficacy by PTX-loaded PEGylated poly(ɛ-caprolactone) nanoparticles: In vitro and in vivo evaluation.

    abstract::The aim of this work was to investigate the anti-tumor effect of paclitaxel (PTX)-loaded methoxy poly(ethylene glycol)-poly(ɛ-caprolactone) nanoparticles (MPEG-NP/PTX) against glioblastoma multiforme (GBM). MPEG-NP/PTX was prepared by the emulsion and evaporation technique with particle size of 72.5±2.2nm and did not ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.10.005

    authors: Xin H,Chen L,Gu J,Ren X,Wei Z,Luo J,Chen Y,Jiang X,Sha X,Fang X

    更新日期:2010-12-15 00:00:00

  • Evaluation of HO-1-u-1 cell line as an in vitro model for sublingual drug delivery involving passive diffusion--Initial validation studies.

    abstract::The aim of this study was to provide preliminary validation of a new sublingual mucosal cell line (HO-1-u-1) for use as in vitro sublingual drug delivery screening of compounds involving passive diffusion. HO-1-u-1 cells were seeded on cell culture inserts. The ultrastructure and integrity of cell layers, inter-passag...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.10.012

    authors: Wang Y,Zuo Z,Lee KK,Chow MS

    更新日期:2007-04-04 00:00:00

  • Compression of pellets coated with various aqueous polymer dispersions.

    abstract::Pellets coated with a new aqueous polyvinyl acetate dispersion, Kollicoat SR 30 D, could be compressed into tablets without rupture of the coating providing unchanged release profiles. In contrast, the compression of pellets coated with the ethylcellulose dispersion, Aquacoat ECD 30, resulted in rupture of the coating...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.03.019

    authors: Dashevsky A,Kolter K,Bodmeier R

    更新日期:2004-07-26 00:00:00

  • Strain-specific differences in behaviour among Lacticaseibacillus rhamnosus cell wall mutants during direct compression.

    abstract::The human body harbours a large variety of microbial communities. It is already well-known that these communities play an important role in human health. Therefore, microbial imbalances can be responsible for several health disorders by different mechanisms. In recent years, probiotic bacteria have been increasingly a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119755

    authors: Byl E,Jokicevic K,Kiekens S,Lebeer S,Kiekens F

    更新日期:2020-10-15 00:00:00

  • Controlled dual release of basic fibroblast growth factor and indomethacin from heparin-conjugated polymeric micelle.

    abstract::This work describes the development of heparinized polymeric micelle as a novel injectable carrier for the dual drug delivery that can simultaneously release basic fibroblast growth factor (bFGF) and indomethacin (IMC), which can promote the regeneration of damaged tissue and prevent the inflammatory response after im...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.06.025

    authors: Lee JS,Bae JW,Joung YK,Lee SJ,Han DK,Park KD

    更新日期:2008-01-04 00:00:00

  • Discrete particle modeling and micromechanical characterization of bilayer tablet compaction.

    abstract::A mechanistic particle scale model is proposed for bilayer tablet compaction. Making bilayer tablets involves the application of first layer compaction pressure on the first layer powder and a second layer compaction pressure on entire powder bed. The bonding formed between the first layer and the second layer particl...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.07.032

    authors: Yohannes B,Gonzalez M,Abebe A,Sprockel O,Nikfar F,Kiang S,Cuitiño AM

    更新日期:2017-08-30 00:00:00

  • Pharmacokinetic study of a carbamazepine nanoemulsion in beagle dogs.

    abstract::This work describes the pharmacokinetics of a novel carbamazepine nanoemulsion. The plasma concentration profiles were determined in beagle dogs after i.v. bolus administration of a 5 mg/kg carbamazepine nanoemulsion and compared to the corresponding carbamazepine/hydroxypropyl-beta-cyclodextrin complex solution. Both...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2009.05.055

    authors: Kuminek G,Kratz JM,Ribeiro R,Kelmann RG,de Araújo BV,Teixeira HF,Simões CM,Koester LS

    更新日期:2009-08-13 00:00:00

  • Dispersibility of lactose fines as compared to API in dry powders for inhalation.

    abstract::This work investigates the dispersion performance of fine lactose particles as function of processing time, and compares it to the API, using Beclomethasone Dipropionate (BDP) as model API. The total load of fine particles is kept constant in the formulations while the proportions of API and lactose fines are varied. ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.03.004

    authors: Thalberg K,Åslund S,Skogevall M,Andersson P

    更新日期:2016-05-17 00:00:00

  • Preparation of nimodipine-loaded microemulsion for intranasal delivery and evaluation on the targeting efficiency to the brain.

    abstract::The purpose of this study was to improve the solubility and enhance the brain uptake of nimodipine (NM) in an o/w microemulsion, which was suitable for intranasal delivery. Three microemulsion systems stabilized by the nonionic surfactants either Cremophor RH 40 or Labrasol, and containing a variety of oils, namely is...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.01.039

    authors: Zhang Q,Jiang X,Jiang W,Lu W,Su L,Shi Z

    更新日期:2004-05-04 00:00:00

  • Effects of polyamidoamine (PAMAM) dendrimers on the nasal absorption of poorly absorbable drugs in rats.

    abstract::The absorption enhancing effects of polyamidoamine (PAMAM) dendrimers with various concentrations and generations on the nasal absorption of fluorescein isothiocyanate-labeled dextran with an average molecular weight of 4400 (FD4) were initially studied in rats. PAMAM dendrimers with different generations improved the...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.04.021

    authors: Dong Z,Katsumi H,Sakane T,Yamamoto A

    更新日期:2010-06-30 00:00:00

  • Quantifying electrostatic interactions in pharmaceutical solid systems.

    abstract::Triboelectrification of pharmaceutical powders with stainless steel and polymer contact surfaces was investigated. alpha-Lactose monohydrate, from 90 to 125 up to 355-500 microm, was used to quantify electrostatic interactions with negligible powder adhesion to the contact surface. Size fractions down to 53-75 microm ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(01)00784-0

    authors: Rowley G

    更新日期:2001-10-04 00:00:00

  • Marinosomes, marine lipid-based liposomes: physical characterization and potential application in cosmetics.

    abstract::Marinosomes are liposomes based on a natural marine lipid extract containing a high polyunsaturated fatty acid (PUFA) ratio. They were prepared and characterized in conditions that mimic that of topical application in terms of pH, temperature and calcium. Marinosomes were stable in storage conditions for 1 month. At l...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00217-x

    authors: Moussaoui N,Cansell M,Denizot A

    更新日期:2002-08-21 00:00:00

  • Characterization of the coating and tablet core roughness by means of 3D optical coherence tomography.

    abstract::This study demonstrates the use of optical coherence tomography (OCT) to simultaneously characterize the roughness of the tablet core and coating of pharmaceutical tablets. OCT is a high resolution non-destructive and contactless imaging methodology to characterize structural properties of solid dosage forms. Besides ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.12.023

    authors: Markl D,Wahl P,Pichler H,Sacher S,Khinast JG

    更新日期:2018-01-30 00:00:00

  • Glycyrrhizic acid as a multifunctional drug carrier - From physicochemical properties to biomedical applications: A modern insight on the ancient drug.

    abstract::Glycyrrhizic acid is the main active component of Licorice root which has been known in traditional Chinese and Japanese medicine since ancient times. In these cultures glycyrrhizic acid (GA) is one of the most frequently used drugs. However, only in 21-st century a novel unusual property of the GA to enhance the acti...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2019.01.047

    authors: Selyutina OY,Polyakov NE

    更新日期:2019-03-25 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

  • Prolonged analgesic effect of PLGA-encapsulated bee venom on formalin-induced pain in rats.

    abstract::To enhance the medicinal activity of bee venom (BV) acupuncture, bee venom was loaded into biodegradable poly(D,L-lactide-co-glycolide) nanoparticles (BV-PLGA-NPs) by a water-in-oil-in-water-emulsion/solvent-evaporation technique. Rat formalin tests were performed after subcutaneous injection of BV-PLGA-NPs to the Zus...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2009.06.034

    authors: Jeong I,Kim BS,Lee H,Lee KM,Shim I,Kang SK,Yin CS,Hahm DH

    更新日期:2009-10-01 00:00:00