Investigation of L-leucine in reducing the moisture-induced deterioration of spray-dried salbutamol sulfate power for inhalation.

Abstract:

:The aim of this study was to investigate the ability of L-leucine (LL) in preventing moisture-induced deterioration in the in vitro aerosolization performance of spray-dried (SD) salbutamol sulfate (SS). Increasing mass fraction of LL (5-80%) were co-spray dried with SS, and the physicochemical properties of the powders were characterized by laser diffraction, X-ray powder diffraction (XRD) and dynamic vapour sorption (DVS). Furthermore, the surface morphology and chemistry of fine particles was analyzed by scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). The in vitro aerosolization performance of powders stored at different relative humidity (RH) was evaluated by a next generation impactor (NGI). The SD SS powders were moderately hygroscopic and amorphous, of which the uptake of moisture upon storage caused a drop in the aerosolization performance. The results showed that 40% (w/w) LL was sufficient to eliminate the effect of moisture on the aerosolization performance at 60% RH. The formulation containing 40% (w/w) LL also maximized the aerosolization performance of SD SS powders (stored in desiccator) with the emitted fraction being 90.0±1.8%, and the fine particle fraction based on the recovered dose (FPFrecovered) and emitted dose (FPFemitted) being 78.0±3.7% and 86.6±2.9%, respectively. The underlying mechanisms were that the crystalline LL increased the degree of particle surface corrugation, and reduced particle fusion and cohesiveness to facilitate dispersion. However, there is still a great challenge to prevent the moisture-induced deterioration in the aerosolization performance at 75% RH due to the recrystallization of SD SS. In conclusion, LL is a potential excipient for reducing moisture-induced deterioration in the aerosolization performance of SD amorphous powders, but still has drawbacks in preventing the recrystallization-induced deterioration.

journal_name

Int J Pharm

authors

Li L,Leung SSY,Gengenbach T,Yu J,Gao GF,Tang P,Zhou QT,Chan HK

doi

10.1016/j.ijpharm.2017.07.033

subject

Has Abstract

pub_date

2017-09-15 00:00:00

pages

30-39

issue

1-2

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(17)30632-4

journal_volume

530

pub_type

杂志文章
  • Lipid nanovehicles with adjustable surface properties for overcoming multiple barriers simultaneously in oral administration.

    abstract::Lipid nanoparticles (LNs) are widely investigated for oral drug delivery, and for achieving significant advantages in colloidal stability, biocompatibility and scaled-up possibility. However, researchers face challenge of developing methods to improve the ability of LNs in overcoming multiple barriers (i.e., mucus and...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.02.015

    authors: Wu L,Liu M,Shan W,Cui Y,Zhang Z,Huang Y

    更新日期:2017-03-30 00:00:00

  • Enhancing the solubility and permeability of the diuretic drug furosemide via multicomponent crystal forms.

    abstract::Furosemide (FSM) is a biopharmaceutical classification system (BCS) class IV drug, being a potent loop diuretic used in the treatment of congestive heart failure and edema. Due to its low solubility and permeability, FSM is known for exhibiting poor oral bioavailability. In order to overcome or even minimize these und...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119694

    authors: Diniz LF,Carvalho PS Jr,Pena SAC,Gonçalves JE,Souza MAC,de Souza Filho JD,Bomfim Filho LFO,Franco CHJ,Diniz R,Fernandes C

    更新日期:2020-09-25 00:00:00

  • Silica nanoparticle coated liposomes: a new type of hybrid nanocapsule for proteins.

    abstract::A hybrid silica-liposome nanocapsule system containing insulin has been developed and the encapsulation, protection and release properties are evaluated. The formulation strategy is based on using insulin-loaded 1,2-dipalmitoyl-sn-glycero-3-phosphocholine and cholesterol liposomes as a template for the deposition of i...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.03.061

    authors: Mohanraj VJ,Barnes TJ,Prestidge CA

    更新日期:2010-06-15 00:00:00

  • Co-delivery of zinc and 5-aminosalicylic acid from alginate/N-succinyl-chitosan blend microspheres for synergistic therapy of colitis.

    abstract::The present study developed novel zinc ion cross-linked alginate/N-succinyl-chitosan (NSC) blend microspheres (MS) for co-delivery of zinc and 5-aminosalicylic acid (5-ASA) for synergistic therapy of colitis. Physicochemical characterization of blend MS was assessed using scanning electron microscopy (SEM), Fourier tr...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.11.036

    authors: Duan H,Lü S,Qin H,Gao C,Bai X,Wei Y,Wu X,Liu M,Zhang X,Liu Z

    更新日期:2017-01-10 00:00:00

  • Investigating the role of cholesterol in the formation of non-ionic surfactant based bilayer vesicles: thermal analysis and molecular dynamics.

    abstract::The aim of this research was to investigate the molecular interactions occurring in the formulation of non-ionic surfactant based vesicles composed monopalmitoyl glycerol (MPG), cholesterol (Chol) and dicetyl phosphate (DCP). In the formulation of these vesicles, the thermodynamic attributes and surfactant interaction...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.11.063

    authors: Wilkhu JS,Ouyang D,Kirchmeier MJ,Anderson DE,Perrie Y

    更新日期:2014-01-30 00:00:00

  • Water solubilization capacity of pharmaceutical microemulsions based on Peceol®, lecithin and ethanol.

    abstract::Biocompatible microemulsions composed of Peceol(®), lecithin, ethanol and water developed for encapsulation of hydrophilic drugs were investigated. The binary mixture Peceol(®)/ethanol was studied first. It was shown that the addition of ethanol to pure Peceol(®) has a significant fluidifying and disordering effect on...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.07.018

    authors: Mouri A,Diat O,Lerner DA,El Ghzaoui A,Ajovalasit A,Dorandeu C,Maurel JC,Devoisselle JM,Legrand P

    更新日期:2014-11-20 00:00:00

  • Characterization of physico-chemical properties and pharmaceutical performance of sucrose co-freeze-dried solid nanoparticulate powders of the anti-HIV agent loviride prepared by media milling.

    abstract::In order to improve the dissolution and absorption properties of loviride, a poorly soluble antiviral agent, sucrose co-freeze-dried nanopowders were prepared, characterized and evaluated. Tween 80/poloxamer 188-stabilized nanosuspensions were produced on a laboratory scale using media milling. The milling process was...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.02.005

    authors: Van Eerdenbrugh B,Froyen L,Martens JA,Blaton N,Augustijns P,Brewster M,Van den Mooter G

    更新日期:2007-06-29 00:00:00

  • Mucoadhesive zein/beta-cyclodextrin nanoparticles for the buccal delivery of curcumin.

    abstract::Herein, we have developed sprayable dispersions of mucoadhesive nanoparticles (NPs) made of zein, a hydrophobic plant-based protein, for the buccal delivery of curcumin (CUR), a poorly water-soluble polyphenol. NPs were prepared by the liquid-liquid dispersion method using an antisolvent water solution without or with...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119587

    authors: Esposito D,Conte C,d'Angelo I,Miro A,Ungaro F,Quaglia F

    更新日期:2020-08-30 00:00:00

  • Physical ageing and thermal analysis of PLGA microspheres encapsulating protein or DNA.

    abstract::PLGA microspheres undergo physical ageing but their ageing kinetics have not been reported, nor the effect of encapsulated protein or plasmid DNA on any associated changes to the glass transition. Differential scanning calorimetry (DSC) was used to measure the rate of ageing of various PLGA microsphere formulations, w...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.02.026

    authors: Rouse JJ,Mohamed F,van der Walle CF

    更新日期:2007-07-18 00:00:00

  • What level of protection can be obtained using sun protective clothing? Determining effectiveness using an in vitro method.

    abstract::It has been clearly demonstrated that ultraviolet radiation is harmful to the skin and can cause helioderma and cancers. There are different methods of combating ultraviolet radiation: sunscreens formulated with filters and/or screens as well as clothing. For this work, the authors studied different fabrics to evaluat...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.06.022

    authors: Ghazi S,Couteau C,Coiffard LJ

    更新日期:2010-09-15 00:00:00

  • Human erythrocytes are affected in vitro by flavonoids of Aristotelia chilensis (Maqui) leaves.

    abstract::Aristotelia chilensis (Mol.) Stuntz (A. chilensis), also known as maqui, is a plant of the Elaeocarpaceae family that grows in central and southern Chile as well as southwestern Argentina. Infusions of its leaves have long been used in the traditional native herbal medicine to treat different ailments. Phytochemical s...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.07.005

    authors: Suwalsky M,Vargas P,Avello M,Villena F,Sotomayor CP

    更新日期:2008-11-03 00:00:00

  • Tumor targeted delivery of octreotide-periplogenin conjugate: Synthesis, in vitro and in vivo evaluation.

    abstract::Periplogenin (PPG), a cardiac glycoside prepared from Cortex periplocae, with similar structure to bufalin, has been found to induce apoptosis in many tumor cells. However, lots of cardiac glycosides possessing strong antitumor activity in vitro have still not passed phase I clinical trials, mostly due to poor tumor s...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.02.024

    authors: Zhang HY,Xu WQ,Wang YW,Omari-Siaw E,Wang Y,Zheng YY,Cao X,Tong SS,Yu JN,Xu XM

    更新日期:2016-04-11 00:00:00

  • Inertial sizing of aerosol inhaled from two dry powder inhalers with realistic breath patterns versus constant flow rates.

    abstract::A procedure is developed that allows particles inhaled with realistic breath patterns to be sized by cascade impaction at a constant flow rate. This procedure is then used to examine the difference between particle sizes obtained with constant flow rate (step profile) versus actual-subject breath patterns for two dry ...

    journal_title:International journal of pharmaceutics

    pub_type: 临床试验,杂志文章

    doi:10.1016/s0378-5173(00)00569-x

    authors: Finlay WH,Gehmlich MG

    更新日期:2000-12-04 00:00:00

  • The influence of the physicochemical characteristics and pharmacokinetic properties of selected NSAID's on their transdermal absorption.

    abstract::The purpose of this study was to determine the plasma concentrations of selected NSAIDs after topical gel administration and to determine the influence of the physicochemical characteristics of these drugs on transdermal absorption. Plasma concentrations of the drugs were determined using high performance liquid chrom...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00340-3

    authors: Beetge E,du Plessis J,Müller DG,Goosen C,van Rensburg FJ

    更新日期:2000-01-05 00:00:00

  • Facile synthesis of pH sensitive polymer-coated mesoporous silica nanoparticles and their application in drug delivery.

    abstract::pH-responsive polymer shell chitosan/poly (methacrylic acid) (CS-PMAA) was coated on mesoporous silica nanoparticles (MSN) through the facile in situ polymerization method. The resultant composite microspheres showed a flexible control over shell thickness, surface charges and hydrodynamic size by adjusting the feedin...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.10.013

    authors: Tang H,Guo J,Sun Y,Chang B,Ren Q,Yang W

    更新日期:2011-12-15 00:00:00

  • Buccal absorption of ergotamine tartrate using the bioadhesive tablet system in guinea-pigs.

    abstract::The buccal administration of ergotamine tartrate (ET) combined with polyvinyl alcohol (PVA) gel brought about higher plasma concentration of ET compared with that of oral administration of capsules in guinea-pigs. T(max) of ET in plasma of buccal administration was significantly smaller than that of oral administratio...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00070-4

    authors: Tsutsumi K,Obata Y,Nagai T,Loftsson T,Takayama K

    更新日期:2002-05-15 00:00:00

  • Glycerosomes: Investigation of role of 1,2-dimyristoyl-sn-glycero-3-phosphatidycholine (DMPC) on the assembling and skin delivery performances.

    abstract::Glycerosomes were formulated using 1,2-dimyristoyl-sn-glycero-3-phosphatidycholine (DMPC), diclofenac sodium salt and 10, 20 or 30% glycerol in the water phase, while corresponding liposomes were prepared with the same amount of DMPC and diclofenac, without glycerol. The aim of the present work was to evaluate the eff...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.09.026

    authors: Manca ML,Manconi M,Zaru M,Valenti D,Peris JE,Matricardi P,Maccioni AM,Fadda AM

    更新日期:2017-10-30 00:00:00

  • Downregulation of survivin expression and enhanced chemosensitivity of MCF-7 cells to adriamycin by PDMAE/survivin shRNA complex nanoparticles.

    abstract::Gene silencing mediated by RNA interference (RNAi) presents a promising strategy for gene therapy. The aim of this work is to evaluate a new gene delivery system for downregulation of survivin expression and enhanced chemosensitivity of MCF-7 cells to adriamycin (ADR). A new cationic poly(2-dimethylaminoethylamine/2-(...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.11.047

    authors: Yang Y,Gao Y,Chen L,Huang Y,Li Y

    更新日期:2011-02-28 00:00:00

  • Effects of permeation enhancers on flufenamic acid delivery in Ex vivo human skin by confocal Raman microscopy.

    abstract::For effective topical delivery, a drug must cross the stratum corneum (SC) barrier into viable tissue. The use of permeation enhancers is a widespread approach for barrier modification. In the current study, flufenamic acid (FluA), a non-steroidal anti-inflammatory drug, is a model agent for investigating the influenc...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.04.011

    authors: Pyatski Y,Zhang Q,Mendelsohn R,Flach CR

    更新日期:2016-05-30 00:00:00

  • Self-nanoemulsifying drug delivery system of persimmon leaf extract: Optimization and bioavailability studies.

    abstract::In current study, a self-nanoemulsifying drug delivery system (SNEDDS) of persimmon (Diospyros kaki) leaf extract (PLE) was developed and characterized to compare its in vitro dissolution and relative bioavailability with commercially available tablets (Naoxinqing tablets). Pseudo-ternary phase diagrams were construct...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.08.024

    authors: Li W,Yi S,Wang Z,Chen S,Xin S,Xie J,Zhao C

    更新日期:2011-11-25 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

  • Designing optimal formulations for hot-melt coating.

    abstract::Hot-melt coating (HMC) as a solvent-free technology grants faster and more economic coating processes with reduced risk of dissolving the drug during the process. Moreover, traditional coating equipment can be modified to enable the HMC process. Despite the indubitable advantages and feasibility of the process, HMC is...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.08.086

    authors: Lopes DG,Salar-Behzadi S,Zimmer A

    更新日期:2017-11-30 00:00:00

  • The degradation of N,N',N"-triethylenephosphoramide in aqueous solutions: a qualitative and kinetic study.

    abstract::The degradation of N,N',N"-triethylenephosphoramide (TEPA) in aqueous solutions has been investigated over a pH range of 3-14. Samples were analyzed using a gas chromatographic system with nitrogen/phosphorus selective detection. The degradation kinetics were studied as function of pH, sodium chloride concentration an...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00444-5

    authors: van Maanen RJ,Tijhof IM,Damen JM,Zwikker JW,Beijnen JH

    更新日期:2000-02-25 00:00:00

  • Poly(ethylene glycol) layered silicate nanocomposites for retarded drug release prepared by hot-melt extrusion.

    abstract::Composites of paracetamol loaded poly(ethylene glycol) (PEG) with a naturally derived and partially synthetic layered silicate (nanoclay) were prepared using hot-melt extrusion. The extent of dispersion and distribution of the paracetamol and nanoclay in the PEG matrix was examined using a combination of field emissio...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.06.027

    authors: Campbell K,Craig DQ,McNally T

    更新日期:2008-11-03 00:00:00

  • Fabrication and structure analysis of poly(lactide-co-glycolic acid)/silk fibroin hybrid scaffold for wound dressing applications.

    abstract::Silk fibroin (SF) and poly(lactide-co-glycolic acid) (PLGA) have been proved to be invaluable polymers in the field wound healing. This study aims at optimizing the electrospinning process of those polymers to make a hybrid membrane as a chronic wounds dressing. After characterizing the scaffolds, PLGA/SF (2:1), and P...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.07.021

    authors: Shahverdi S,Hajimiri M,Esfandiari MA,Larijani B,Atyabi F,Rajabiani A,Dehpour AR,Gharehaghaji AA,Dinarvand R

    更新日期:2014-10-01 00:00:00

  • Improved plasma stability and sustained release profile of gemcitabine via polypeptide conjugation.

    abstract::To enhance the stability of the anticancer drug gemcitabine (2'-deoxy-2',2'-difluorocytidine), it was conjugated to poly-l-glutamic acid (PG-H) via a carbodiimide reaction. The synthesised poly-l-glutamic acid-gemcitabine (PG-G) was purified and characterised by using SDS-PAGE to estimate its molecular weight, HPLC to...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.03.010

    authors: Kiew LV,Cheong SK,Sidik K,Chung LY

    更新日期:2010-05-31 00:00:00

  • Co-former selection for co-amorphous drug-amino acid formulations.

    abstract::We have previously developed a fast screening method on the ability of twenty amino acids (AA) to form co-amorphous formulations with six drugs upon ball milling. In this work, the potential advantages in physical stability and dissolution rate of the 36 successful co-amorphous formulations, compared to the pure amorp...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.12.036

    authors: Kasten G,Löbmann K,Grohganz H,Rades T

    更新日期:2019-02-25 00:00:00

  • In vitro and in vivo evaluation of a melamine dendrimer as a vehicle for drug delivery.

    abstract::Cell-based and acute and subchronic in vivo toxicity profiles of a dendrimer based on melamine reveal that this class of molecules warrants additional study as vehicles for drug delivery. In cell culture, a substantial decrease in viability was observed at 0.1 mg/mL. For the acute studies, mice were administered 2.5, ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2004.04.023

    authors: Neerman MF,Zhang W,Parrish AR,Simanek EE

    更新日期:2004-08-20 00:00:00

  • A system for the production and delivery of monodisperse salbutamol aerosols to the lungs.

    abstract::An aerosol system is described for the generation and delivery of measured doses of monodisperse therapeutic drug particles to the human lungs. The system comprises a spinning top aerosol generator (STAG), aerosol chamber and inhalation control unit. Monodisperse aerosols allow drug particle size effects to be studied...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(03)00032-2

    authors: Biddiscombe MF,Usmani OS,Barnes PJ

    更新日期:2003-03-26 00:00:00

  • A theoretical approach to evaluate the release rate of acetaminophen from erosive wax matrix dosage forms.

    abstract::To predict drug dissolution and understand the mechanisms of drug release from wax matrix dosage forms containing glyceryl monostearate (GM; a wax base), aminoalkyl methacrylate copolymer E (AMCE; a pH-dependent functional polymer), and acetaminophen (APAP; a model drug), we tried to derive a novel mathematical model ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.05.015

    authors: Agata Y,Iwao Y,Shiino K,Miyagishima A,Itai S

    更新日期:2011-07-29 00:00:00