Terahertz pulsed imaging as an advanced characterisation tool for film coatings--a review.

Abstract:

:Solid dosage forms are the pharmaceutical drug delivery systems of choice for oral drug delivery. These solid dosage forms are often coated to modify the physico-chemical properties of the active pharmaceutical ingredients (APIs), in particular to alter release kinetics. Since the product performance of coated dosage forms is a function of their critical coating attributes, including coating thickness, uniformity, and density, more advanced quality control techniques than weight gain are required. A recently introduced non-destructive method to quantitatively characterise coating quality is terahertz pulsed imaging (TPI). The ability of terahertz radiation to penetrate many pharmaceutical materials enables structural features of coated solid dosage forms to be probed at depth, which is not readily achievable with other established imaging techniques, e.g. near-infrared (NIR) and Raman spectroscopy. In this review TPI is introduced and various applications of the technique in pharmaceutical coating analysis are discussed. These include evaluation of coating thickness, uniformity, surface morphology, density, defects and buried structures as well as correlation between TPI measurements and drug release performance, coating process monitoring and scale up. Furthermore, challenges and limitations of the technique are discussed.

journal_name

Int J Pharm

authors

Haaser M,Gordon KC,Strachan CJ,Rades T

doi

10.1016/j.ijpharm.2013.03.053

subject

Has Abstract

pub_date

2013-12-05 00:00:00

pages

510-20

issue

2

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(13)00283-4

journal_volume

457

pub_type

杂志文章,评审
  • Oral delivery of oleuropein-loaded lipid nanocarriers alleviates inflammation and oxidative stress in acute colitis.

    abstract::Inflammation and oxidative stress pathways have emerged as novel targets in the management of inflammatory bowel diseases (IBD). Targeting the drug to the inflamed colon remains a challenge. Nanostructured lipid carriers (NLCs) have been reported to accumulate in inflamed colonic mucosa. The antioxidant/antiinflamator...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119515

    authors: Huguet-Casquero A,Xu Y,Gainza E,Pedraz JL,Beloqui A

    更新日期:2020-08-30 00:00:00

  • Drug release modeled by dissolution, diffusion, and immobilization.

    abstract::This article presents a novel drug release model that combines drug dissolution, diffusion, and immobilization caused by adsorption of the drug to the tablet constituents. Drug dissolution is described by the well-known Noyes-Whitney equation and drug adsorption by a Langmuir-Freundlich adsorption isotherm, and these ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00539-2

    authors: Frenning G,Strømme M

    更新日期:2003-01-02 00:00:00

  • Enabling real time release testing by NIR prediction of dissolution of tablets made by continuous direct compression (CDC).

    abstract::A method for predicting dissolution profiles of directly compressed tablets for a fixed sustained release formulation manufactured in a continuous direct compaction (CDC) system is presented. The methodology enables real-time release testing (RTRt). Tablets were made at a target drug concentration of 9% Acetaminophen,...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.08.033

    authors: Pawar P,Wang Y,Keyvan G,Callegari G,Cuitino A,Muzzio F

    更新日期:2016-10-15 00:00:00

  • Degradable dextran microspheres for the controlled release of liposomes.

    abstract::A novel delivery concept based on the encapsulation of liposomes in biodegradable dextran microspheres was developed. The microspheres were prepared using a two-phase system, consisting of water/poly(ethylene glycol), and water/methacrylated dextran. Liposomes were encapsulated almost quantitatively and in their intac...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(00)00625-6

    authors: Stenekes RJ,Loebis AE,Fernandes CM,Crommelin DJ,Hennink WE

    更新日期:2001-02-19 00:00:00

  • Broad spectrum bioactive sunscreens.

    abstract::The development of sunscreens containing reduced concentration of chemical UV filters, even though, possessing broad spectrum effectiveness with the use of natural raw materials that improve and infer UV absorption is of great interest. Due to the structural similarities between polyphenolic compounds and organic UV f...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.06.031

    authors: Velasco MV,Sarruf FD,Salgado-Santos IM,Haroutiounian-Filho CA,Kaneko TM,Baby AR

    更新日期:2008-11-03 00:00:00

  • Inhalable liposomal formulation for vasoactive intestinal peptide.

    abstract::Inhalation of vasoactive intestinal peptide (VIP) was suggested as promising treatment option of various lung diseases like asthma and pulmonary hypertension. However, the medical use of peptides is limited by their short half-life due to rapid enzymatic degradation in the airways. For that reason, we recently develop...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.01.046

    authors: Hajos F,Stark B,Hensler S,Prassl R,Mosgoeller W

    更新日期:2008-06-05 00:00:00

  • Green fabricated reduced graphene oxide: evaluation of its application as nano-carrier for pH-sensitive drug delivery.

    abstract::A green and mild approach for the preparation of reduced graphene oxide (rGO) was proposed by using riboflavin-5'-phosphate sodium salt dihydrate as a reducing reagent and stabilizer without any other reagent. The fabricated nano-rGO was systematically evaluated for its application as nano-carrier for pH-sensitive dru...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.10.081

    authors: Ma N,Zhang B,Liu J,Zhang P,Li Z,Luan Y

    更新日期:2015-12-30 00:00:00

  • Dissolution of fine particle fraction from truncated Anderson cascade impactor with an enhancer cell.

    abstract::Dissolution testing for inhalers were previously conducted either on unfractionated drug-carrier powders or drug of specific aerodynamic particle size. In this study, the collection of the full fine particle fraction (FPF) was attempted on a single stage. Capsules containing 30 mg of 2% salbutamol sulfate (SS) was tes...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.04.048

    authors: Tay JYS,Liew CV,Heng PWS

    更新日期:2018-07-10 00:00:00

  • GSH responsive nanomedicines self-assembled from small molecule prodrug alleviate the toxicity of cardiac glycosides as potent cancer drugs.

    abstract::Cardiac glycosides (CGs) have been used to treat cancer for hundreds of years. However, the narrow therapeutic window and system toxicity have hindered their wide clinical applications. Herein, the small molecule prodrug strategy and nanotechnology were integrated into one drug delivery system with enhanced therapeuti...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.118980

    authors: Zhang H,Zhu Y,Sun C,Xie Y,Adu-Frimpong M,Deng W,Yu J,Xu X,Han Z,Qi G

    更新日期:2020-02-15 00:00:00

  • Prediction of oral absorption in humans by experimental immobilized artificial membrane chromatography indices and physicochemical descriptors.

    abstract::The purpose of the present study was to examine the human oral absorption (HOA) predictability of the experimentally determined immobilized artificial membrane (IAM) chromatography capacity factor (log k'IAM) in conjunction with physicochemical descriptors. Transcellular permeation was modeled based on determination o...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.04.025

    authors: Kotecha J,Shah S,Rathod I,Subbaiah G

    更新日期:2008-08-06 00:00:00

  • Cell uptake, cytoplasmic diffusion and nuclear access of a 6.5 nm diameter dendrimer.

    abstract::Macromolecular crowding and the presence of organelles in the cytosol present barriers to particle mobility, such that it is unclear how nano-carriers can deliver their active agents to the nucleus. In this work a sixth generation amino terminated polyamide polylysine dendrimer (Gly-Lys(63) (NH(2))(64)) (MW 8149, diam...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.12.012

    authors: Ruenraroengsak P,Al-Jamal KT,Hartell N,Braeckmans K,De Smedt SC,Florence AT

    更新日期:2007-03-01 00:00:00

  • Impact of implant composition of twin-screw extruded lipid implants on the release behavior.

    abstract::The development of vaccine delivery systems that will remove or reduce the need for repeated dosing has led to the investigation of sustained release systems. In this context, the duration of antigen release is of great importance as is the requirement for concomitant adjuvant release. In this work, lipid implants con...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.06.052

    authors: Even MP,Bobbala S,Kooi KL,Hook S,Winter G,Engert J

    更新日期:2015-09-30 00:00:00

  • Colonic metabolism of ranitidine: implications for its delivery and absorption.

    abstract::The aim of this study was to assess the in vitro stability of ranitidine to colonic bacteria by utilising a batch culture fermentation system to simulate the conditions of the colon. Three quantities of ranitidine, 100, 200 and 500 mg, in the form of the hydrochloride salt, were introduced into individual 100 ml ferme...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(01)00794-3

    authors: Basit AW,Lacey LF

    更新日期:2001-10-04 00:00:00

  • Air classifier technology (ACT) in dry powder inhalation. Part 2. The effect of lactose carrier surface properties on the drug-to-carrier interaction in adhesive mixtures for inhalation.

    abstract::The effect of carrier surface properties on drug particle detachment from carrier crystals during inhalation with a special test inhaler with basic air classifier has been studied for mixtures containing 0.4% budesonide. Carrier crystals were retained in the classifier during inhalation and subsequently examined for t...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(03)00264-3

    authors: de Boer AH,Hagedoorn P,Gjaltema D,Goede J,Kussendrager KD,Frijlink HW

    更新日期:2003-07-24 00:00:00

  • Development of enteric-coated fixed dose combinations of amorphous solid dispersions of ezetimibe and lovastatin: Investigation of formulation and process parameters.

    abstract::Enteric-coated fixed-dose combinations of ezetimibe and lovastatin were prepared by fluid bed coating aiming to avoid the acidic conversion of lovastatin to its hydroxyacid derivative. In a two-step process, sucrose beads were layered with a glass solution of ezetimibe, lovastatin and Soluplus®, top-coated with an ent...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.01.053

    authors: Riekes MK,Dereymaker A,Berben P,Augustijns P,Stulzer HK,Van den Mooter G

    更新日期:2017-03-30 00:00:00

  • Physicochemical characteristics of quinupramine in the EVA matrix.

    abstract::Ethylene-vinyl acetate (EVA) is widely used as a membrane or matrix for transdermal drug delivery systems. In an attempt to determine the state of a drug in the EVA matrix, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and thermal analysis of the quinupramine-EVA matrix were carried out and ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.06.016

    authors: Cho CW,Choi JS,Shin SC

    更新日期:2006-08-31 00:00:00

  • Distribution of salicylic acid in human stratum corneum following topical application in vivo: a comparison of six different formulations.

    abstract::Distribution of salicylic acid in human stratum corneum from treatment of six different formulations was assessed by quantitation of drug content in sequentially tape-stripped stratum corneum after a single 2-h dose was applied unoccluded to skin on the ventral forearm of four female subjects. The profile and total am...

    journal_title:International journal of pharmaceutics

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1016/s0378-5173(99)00217-3

    authors: Tsai J,Chuang S,Hsu M,Sheu H

    更新日期:1999-10-25 00:00:00

  • Direct quantification of unencapsulated doxorubicin in liposomal doxorubicin formulations using capillary electrophoresis.

    abstract::To understand the quality, efficacy, and safety of liposomal drugs, it is necessary to develop a robust and accurate method for the separation and the quantification of unencapsulated and liposome-associated drugs (or liposomal encapsulated drugs). Conventional methods involve separation of unencapsulated and liposome...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.07.019

    authors: Ansar SM,Jiang W,Mudalige T

    更新日期:2018-10-05 00:00:00

  • A prototype 'Infucon' device for continuous infusion of microbubbles in vivo.

    abstract::A device for continuous infusion of microbubbles (MBs) 'Infucon' has been designed, constructed and tested on rabbits. The device prevents MBs from flotation and accumulation in the layer directly below the surface in the syringe injection during i.v. application. Homogenous i.v. application of MBs was tested on 16 ma...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.12.026

    authors: Kauerová Z,Lukáč R,Kohout P,Mašek J,Koudelka Š,Plocková J,Vašíčková M,Vlašín M,Turánek J

    更新日期:2013-01-30 00:00:00

  • Polymorphism and stability of ibuprofen/nicotinamide cocrystal: The effect of the crystalline synthesis method.

    abstract::The development over the past decade of design strategies for cocrystal preparation have led to numerous methods for the synthesis of cocrystal without take care of their influence on the precise structure and stability of cocrystalline states. On the other hand the mechanism of cocrystal formation remains widely uncl...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119454

    authors: Guerain M,Guinet Y,Correia NT,Paccou L,Danède F,Hédoux A

    更新日期:2020-06-30 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

  • Protein aggregation--pathways and influencing factors.

    abstract::Proteins generally will tend to aggregate under a variety of environmental conditions in comparison with small drug molecules. The extent of aggregation is dependent on many factors that can be broadly classified as intrinsic (primary, secondary, tertiary or quaternary structure) or extrinsic (environment in which pro...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2010.02.025

    authors: Wang W,Nema S,Teagarden D

    更新日期:2010-05-10 00:00:00

  • Influence of the unloading conditions on capping and lamination: Study on a compaction simulator.

    abstract::Capping and lamination are classical industrial issues that can be challenging during the scale up of solid dosage forms. Previous publications showed that changing the unloading conditions (triaxial decompression, loaded ejection) made it possible to mitigate capping. In the present study, a systematic study of the e...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.118468

    authors: Mazel V,Desbois L,Tchoreloff P

    更新日期:2019-08-15 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 influence of formulation variables on in vitro transfection efficiency and physicochemical properties of chitosan-based polyplexes.

    abstract::The aim of this study was to investigate how a selection of formulation variables affects the in vitro transfection efficiency and physicochemical properties (particle size, zetapotential and chitosan-plasmid association) of chitosan-based polyplexes. Experimental designs in combination with multivariate data analysis...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(03)00301-6

    authors: Romøren K,Pedersen S,Smistad G,Evensen Ø,Thu BJ

    更新日期:2003-08-11 00:00:00

  • Impact of molecular rearrangement of amphiphilic stabilizers on physical stability of itraconazole nanoparticles prepared by flash nanoprecipitation.

    abstract::Flash nanoprecipitation (FNP) is a controlled antisolvent precipitation process that has proven effective for consistent production of drug nanoparticles with a defined mean particle size and narrow particle size distribution. However, physical instability of the generated nanoparticles remains a major challenge in th...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.03.006

    authors: Wan KY,Wong KW,Chow AHL,Chow SF

    更新日期:2018-05-05 00:00:00

  • Skin delivery of oestradiol from lipid vesicles: importance of liposome structure.

    abstract::The aim of this study was to investigate the importance of liposome structure in oestradiol skin delivery as a tool for understanding the delivery mechanism from lipid vesicles. Liposomes of phosphatidylcholine (PC) (1), PC, sodium cholate; 86:14 w/w (II), PC, Span 80; 86.7:13.3 w/w (III) and PC, oleic acid: 84:16 w/w...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(00)00493-2

    authors: El Maghraby GM,Williams AC,Barry BW

    更新日期:2000-08-25 00:00:00

  • Preparation and characterization of Chinese yam polysaccharide PLGA nanoparticles and their immunological activity.

    abstract::This paper first provides that Chinese yam polysaccharide (CYP) is encapsulated by PLGA using a double emulsion solvent evaporation method and aims to screen the optimal preparation of CYP-PLGA nanoparticles (CYPP) using response surface methodology (RSM). The volume ratio of the internal water phase to the organic ph...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.06.130

    authors: Luo L,Zheng S,Huang Y,Qin T,Xing J,Niu Y,Bo R,Liu Z,Huang Y,Hu Y,Liu J,Wu Y,Wang D

    更新日期:2016-09-10 00:00:00

  • Raman mapping of pharmaceuticals.

    abstract::Raman spectroscopy may be implemented through a microscope to provide fine scale axial and lateral chemical maps. The molecular structure of many drugs makes Raman spectroscopy particularly well suited to the investigation of pharmaceutical systems. Chemometric methods currently used to assess bulk Raman spectroscopic...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2010.12.030

    authors: Gordon KC,McGoverin CM

    更新日期:2011-09-30 00:00:00

  • Improved photodynamic activity of porphyrin loaded into nanoparticles: an in vivo evaluation using chick embryos.

    abstract::Hydrophobic porphyrins are potentially interesting molecules for the photodynamic therapy (PDT) of solid cancers or ocular vascularization diseases. Their pharmaceutical development is, however, hampered by their lipophilicity, which renders formulation difficult especially when intravenous administration is needed. E...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.07.029

    authors: Vargas A,Pegaz B,Debefve E,Konan-Kouakou Y,Lange N,Ballini JP,van den Bergh H,Gurny R,Delie F

    更新日期:2004-11-22 00:00:00