Mechanical testing methods for drug-releasing vaginal rings.

Abstract:

:Vaginal rings (VRs) are currently marketed for contraceptive or hormone regulation purposes, and investigationally, have been widely reported for delivery of antiretrovirals to reduce HIV transmission. To date, there is no national or international standard for the mechanical testing and minimum performance characteristics of any VR based products. Here, we describe a series of mechanical tests examining the durometer hardness, static and dynamic compression response, tensile properties and twist resistance of vaginal rings. The tests were conducted on currently marketed VRs and a number of the International Partnership for Microbicides' (IPM) investigational VR formulations. With wider application in the field, the tests described herein could form the basis for a more standardised approach to the mechanical testing of VRs.

journal_name

Int J Pharm

authors

McCoy CF,Millar BG,Murphy DJ,Blanda W,Hansraj B,Devlin B,Malcolm RK,Boyd P

doi

10.1016/j.ijpharm.2019.01.026

subject

Has Abstract

pub_date

2019-03-25 00:00:00

pages

182-191

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(19)30061-4

journal_volume

559

pub_type

杂志文章
  • 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

  • Spherical agglomerates of lactose with enhanced mechanical properties.

    abstract::The aim of this study was to prepare spherical agglomerates of lactose and to evaluate their physicochemical properties, flow properties, particle friability and compaction properties, and to compare them to commercially available types of lactose for direct compression (spray-dried, granulated and anhydrous β-lactose...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.11.040

    authors: Lamešić D,Planinšek O,Lavrič Z,Ilić I

    更新日期:2017-01-10 00:00:00

  • Insulin containing polyethylenimine-dextran sulfate nanoparticles.

    abstract::An aqueous nanoparticle delivery system has been developed which employs the oppositely charged polymers polyethylenimine (PEI) and dextran sulfate (DS) with zinc as a stabilizer. It is found that the pH of PEI solutions, the weight ratio of the two polymers, and zinc sulfate concentrations all play significant roles ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(03)00055-3

    authors: Tiyaboonchai W,Woiszwillo J,Sims RC,Middaugh CR

    更新日期:2003-04-14 00:00:00

  • An improved method for the characterization of supersaturation and precipitation of poorly soluble drugs using pulsatile microdialysis (PMD).

    abstract::In current pharmaceutical drug discovery, most candidates are poorly soluble in water, which can result in poor bioavailability. To overcome this problem, formulations that create supersaturation of the drug are a well-studied alternative. Characterizing the dissolution from these systems is challenging because conven...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.04.012

    authors: Shah KB,Patel PG,Khairuzzaman A,Bellantone RA

    更新日期:2014-07-01 00:00:00

  • Improving long circulation and procoagulant platelet targeting by engineering of hirudin prodrug.

    abstract::To reduce systemic bleeding risks during anticoagulant treatment, a new concept named "precise anticoagulation" was proposed to localize the effects of anticoagulants via the targeted delivery of prodrugs to the coagulation site. In this study, the fusion protein Annexin V-hirudin 3-ABD (hAvHA) was constructed to achi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119869

    authors: Han HH,Zhang HT,Wang R,Yan Y,Liu X,Wang Y,Zhu Y,Wang JC

    更新日期:2020-09-10 00:00:00

  • Can spray freeze-drying improve the re-dispersion of crystalline nanoparticles of pure naproxen?

    abstract::Spray freeze drying (SFD) was used to prepare re-dispersible powders of crystalline, pure-drug nanodispersions of naproxen in lactose and stabilized with hydroxypropyl cellulose. The particle size of the rehydrated powders was determined using static light scattering/Mie analysis. The nanoparticles present in the SFD ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.04.061

    authors: Braig V,Konnerth C,Peukert W,Lee G

    更新日期:2019-06-10 00:00:00

  • Enhancing bioavailability through thermal processing.

    abstract::Formulation intervention, through the application of processing technologies, is a requirement for enabling therapy for the vast majority of drugs. Without these enabling technologies, poorly soluble drugs may not achieve therapeutic concentrations in the blood or tissue of interest. Conversely, freely soluble and/or ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2013.04.042

    authors: Keen JM,McGinity JW,Williams RO 3rd

    更新日期:2013-06-25 00:00:00

  • Methotrexate-loaded biodegradable polymeric micelles for lymphoma therapy.

    abstract::Drug resistance and recurrence are the main clinical challenges in chemotherapy of lymphoma. Methotrexate (MTX), especially high dose MTX (HD MTX), is extensively used to treat some aggressive subtypes of lymphoma, such as Burkitt's lymphoma, in order to overcome drug resistance. But poor solubility of the free drug a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.12.025

    authors: Wang MY,Qu Y,Hu DR,Chen LJ,Shi K,Jia YP,Yi YY,Wei Q,Niu T,Qian ZY

    更新日期:2019-02-25 00:00:00

  • Enhanced oral bioavailability of paclitaxel by D-alpha-tocopheryl polyethylene glycol 400 succinate in mice.

    abstract::Paclitaxel is widely used to treat several types of solid tumors. The commercially available paclitaxel formulation contains Cremophor/ethanol as solubilizers. This study evaluated the effects of D-alpha-tocopheryl polyethylene glycol 400 succinate (TPGS 400) on the oral absorption of paclitaxel in mice. Mice were giv...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.04.013

    authors: Ho PY,Yeh TK,Yao HT,Lin HL,Wu HY,Lo YK,Chang YW,Chiang TH,Wu SH,Chao YS,Chen CT

    更新日期:2008-07-09 00:00:00

  • Relationships between surface free energy, surface texture parameters and controlled drug release in hydrophilic matrices.

    abstract::The study of controlled release and drug release devices has been dominated by considerations of the bulk or average properties of material or devices. Yet the outermost surface atoms play a central role in their performance. The objective of this article has been to characterize the surface of hydrophilic matrix tabl...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.11.054

    authors: Saurí J,Suñé-Negre JM,Díaz-Marcos J,Vilana J,Millán D,Ticó JR,Miñarro M,Pérez-Lozano P,García-Montoya E

    更新日期:2015-01-15 00:00:00

  • Wheat germ agglutinin-grafted lipid nanoparticles: preparation and in vitro evaluation of the association with Caco-2 monolayers.

    abstract::A bioadhesive drug delivery system, wheat germ agglutinin (WGA)-grafted lipid nanoparticles, was developed for the oral delivery of bufalin (a hydrophobic active component extracted from the traditional Chinese medicine Chan'su). The lipid nanoparticles associated with poly(vinyl alcohol) (PVA) were prepared by high-p...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.06.030

    authors: Liu Y,Wang P,Sun C,Feng N,Zhou W,Yang Y,Tan R,Chen Z,Wu S,Zhao J

    更新日期:2010-09-15 00:00:00

  • Preparation of nanomagnetic absorbent for partition coefficient measurement.

    abstract::In this paper, we report a new method based on supercritical carbon dioxide (scCO(2)) to fill and distribute the porous magnetic nanoparticles with n-octanol in a homogeneous manner. The high solubility of n-octanol in scCO(2) and high diffusivity and permeability of the fluid allow efficient delivery of n-octanol int...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.07.031

    authors: Tsang SC,Yu CH,Gao X,Tam KY

    更新日期:2006-12-11 00:00:00

  • Short-term delayed-release microcapsules spraycoated with acrylic terpolymers.

    abstract::A series of poly(ethyl acrylate (EA)/methyl methacrylate (MMA)/2-hydroxyethyl methacrylate (HEMA)) lattices were synthesized to prepare short-term delayed-release microcapsules by employing the Wurster coating process. Latex with a HEMA molar fraction exceeding 60% could not be synthesized as an aqueous suspension due...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.10.020

    authors: Liu D,Ichikawa H,Cui F,Fukumori Y

    更新日期:2006-01-13 00:00:00

  • Preparation and characterization of fentanyl-loaded PLGA microspheres: in vitro release profiles.

    abstract::We developed several kinds of fentanyl-loaded poly(L-lactide-co-glycolide) (PLGA) microspheres (FMS) for sustained release of fentanyl. FMS were prepared by an emulsion solvent-evaporation method. In this study, the influences of several preparation parameters, such as initial drug loading, polymer concentration, and ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(01)00968-1

    authors: Choi HS,Seo SA,Khang G,Rhee JM,Lee HB

    更新日期:2002-03-02 00:00:00

  • Functionalized (poly(ɛ-caprolactone))₂-poly(ethylene glycol) nanoparticles with grafting nicotinic acid as drug carriers.

    abstract::Nicotinic acid was grafted on (poly(ɛ-caprolactone))(2)-poly(ethylene glycol) copolymers that were used for the preparation of nanoparticles with the objectives to monitor particle size and to optimize the drug loading capacity as well as the release profile of the particles. Increasing amounts of grafting nicotinic a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.11.033

    authors: Suksiriworapong J,Sripha K,Kreuter J,Junyaprasert VB

    更新日期:2012-02-28 00:00:00

  • Risperidone solid dispersion for orally disintegrating tablet: its formulation design and non-destructive methods of evaluation.

    abstract::The focus of present investigation was to assess the utility of non-destructive techniques in the evaluation of risperidone solid dispersions (SD) with methyl-β-cyclodextrin (MBCD) and subsequent incorporation of the SD into orally disintegrating tablets (ODT) for a faster release of risperidone. The SD was prepared b...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2010.08.025

    authors: Rahman Z,Zidan AS,Khan MA

    更新日期:2010-11-15 00:00:00

  • The effect of a P123 template in mesopores of mesocellular foam on the controlled-release of venlafaxine.

    abstract::A series of mesocellular foams (MCFs)-based mesoporous silica nanospheres (DH-MCF-P123-n, (n=12, 2, 0.5)) were synthesized as controlled-release deliveries for a typical antidepressant drug, venlafaxine. The foams were 3-(2,3-dihydroxypropoxyl)propyl-grafted and the P123 template partially preserved. We studied the re...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.12.048

    authors: Tang J,Bian Z,Hu J,Xu S,Liu H

    更新日期:2012-03-15 00:00:00

  • Efficient loading of ethionamide in cyclodextrin-based carriers offers enhanced solubility and inhibition of drug crystallization.

    abstract::Ethionamide (ETH) is a second line antitubercular drug suffering from poor solubility in water and strong tendency to crystallize. These drawbacks were addressed by loading ETH in β-cyclodextrin (βCyD)-based carriers. The drug was incorporated in a molecular state avoiding crystallization even for long-term storage an...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.05.041

    authors: Wankar J,Salzano G,Pancani E,Benkovics G,Malanga M,Manoli F,Gref R,Fenyvesi E,Manet I

    更新日期:2017-10-15 00:00:00

  • Prediction of aqueous solubility of drug-like molecules using a novel algorithm for automatic adjustment of relative importance of descriptors implemented in counter-propagation artificial neural networks.

    abstract::In this work, we present a novel approach for the development of models for prediction of aqueous solubility, based on the implementation of an algorithm for the automatic adjustment of descriptor's relative importance (AARI) in counter-propagation artificial neural networks (CPANN). Using this approach, the interpret...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.08.022

    authors: Erić S,Kalinić M,Popović A,Zloh M,Kuzmanovski I

    更新日期:2012-11-01 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

  • Investigation of physicochemical factors affecting the stability of a pH-modulated solid dispersion and a tablet during storage.

    abstract::The stability of solid dispersions (SD) during storage is of concern. We prepared the pH-modulated SD (pSD) and compressed tablets consisting of polyethylene glycol (PEG) 6000 as a carrier, drug and MgO (alkalizer). Telmisartan (TEL), an ionizable poorly water-soluble drug, was chosen as a model drug. The changes in p...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.04.065

    authors: Tran PH,Tran TT,Park JB,Min DH,Choi HG,Han HK,Rhee YS,Lee BJ

    更新日期:2011-07-29 00:00:00

  • Key parameters affecting the initial release (burst) and encapsulation efficiency of peptide-containing poly(lactide-co-glycolide) microparticles.

    abstract::The objective of this study was to identify key variables affecting the initial release (burst) and the encapsulation of leuprolide acetate-containing poly(lactide-co-glycolide) (PLGA) microparticles, which were prepared by the cosolvent evaporation method. Adjusting parameters, which affected the PLGA precipitation k...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.06.004

    authors: Luan X,Skupin M,Siepmann J,Bodmeier R

    更新日期:2006-11-06 00:00:00

  • Synthesis, characterization, in vitro and in vivo evaluation of PEGylated oridonin conjugates.

    abstract::Oridonin (ORI), a diterpenoid compound with promising antitumor activity, was proved to possess potent antileukemia efficacies in vitro and in vivo recently. However, the development and application of ORI was limited by its poor solubility and rapid plasma clearance. The purpose of this study was to solve these probl...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.08.014

    authors: Shen J,Zhang D,Zhao Z,Jia L,Zheng D,Liu G,Hao L,Zhang Q,Tian X,Li C,Guo H

    更新日期:2013-11-01 00:00:00

  • Comparative study on radiolabeling and biodistribution of core-shell silver/polymeric nanoparticles-based theranostics for tumor targeting.

    abstract::A simple and rapid method for radiolabeling of three types of Ag NPs has been performed using 125I isotope, with high labeling yields, >90% without disturbing the optical properties. All the factors affecting labeling yield were studied. In order to monitor the in-vivo tissue uptake of radiolabeled Ag NPs using γ-rays...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.06.044

    authors: Farrag NS,El-Sabagh HA,Al-Mahallawi AM,Amin AM,AbdEl-Bary A,Mamdouh W

    更新日期:2017-08-30 00:00:00

  • Preparation and evaluation of self-nanoemulsified drug delivery systems (SNEDDSs) of matrine based on drug-phospholipid complex technique.

    abstract::To enhance oral bioavailability of matrine, a dedicated and newly emerging drug system called self-nanoemulsifying drug delivery system (SNEDDSs) was developed. Phospholipid complex (MPC) was prepared using solvent-evaporation method to improve the liposolubility of matrine. Solubilization test, infrared spectroscopy ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2009.11.026

    authors: Ruan J,Liu J,Zhu D,Gong T,Yang F,Hao X,Zhang Z

    更新日期:2010-02-15 00:00:00

  • Permeation studies through porcine small intestine of furosemide solutions for personalised paediatric administration.

    abstract::Personalized medicine is a challenging research area in paediatric drug design since no suitable pharmaceutical forms are currently available. Furosemide is an anthranilic acid derivative used in paediatric practice to treat cardiac and pulmonary disorders in premature infants and neonates. However, it is not commerci...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.08.059

    authors: Provenza N,Calpena AC,Mallandrich M,Sánchez A,Egea MA,Clares B

    更新日期:2014-11-20 00:00:00

  • DNA nanostructure-based drug delivery nanosystems in cancer therapy.

    abstract::DNA as a novel biomaterial can be used to fabricate different kinds of DNA nanostructures based on its principle of GC/AT complementary base pairing. Studies have shown that DNA nanostructure is a nice drug carrier to overcome big obstacles existing in cancer therapy such as systemic toxicity and unsatisfied drug effi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2017.09.032

    authors: Wu D,Wang L,Li W,Xu X,Jiang W

    更新日期:2017-11-25 00:00:00

  • The influence of carbohydrate nature and drying methods on the compaction properties and pore structure of new methyl methacrylate copolymers.

    abstract::Methyl methacrylate (MMA) copolymers have recently been proposed as an alternative in controlled-release matrix tablets. The aims of this study were to assess the potential value of these copolymers as direct compression excipients and to investigate relationships between the physical and structural properties of the ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00432-5

    authors: Ferrero C,Jiménez-Castellanos MR

    更新日期:2002-11-06 00:00:00

  • Achieving delayed release of freeze-dried probiotic strains by extrusion, spheronization and fluid bed coating - evaluated using a three-step in vitro model.

    abstract::Intake of probiotics is associated with many health benefits, which has generated an interest in formulating viable probiotic supplements. The present study had two aims. The first aim was to achieve gastrointestinal protection and delayed release of viable probiotics by pelletizing and coating freeze-dried probiotic ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.120022

    authors: Jacobsen NMY,Caglayan I,Caglayan A,Bar-Shalom D,Müllertz A

    更新日期:2020-12-15 00:00:00

  • Dextrin-trypsin and ST-HPMA-trypsin conjugates: enzyme activity, autolysis and thermal stability.

    abstract::Using monomethoxy poly(ethylene glycol) (mPEG)-trypsin conjugates we recently showed that both PEG molecular weight (1100-5000 g/mol) and linker chemistry affect the rate of protein autolysis and thermal stability. These important factors are often overlooked but they can guide the early choice of optimal polymer/chem...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2009.02.008

    authors: Treetharnmathurot B,Dieudonné L,Ferguson EL,Schmaljohann D,Duncan R,Wiwattanapatapee R

    更新日期:2009-05-21 00:00:00