Evaluation of the effect of rifampicin on the biophysical properties of the membranes: significance for therapeutic and side effects.

Abstract:

:This work aims to study the biophysical interactions of rifampicin (RIF) with three-dimensional macrophage membrane models, under environments with physiological and pathological relevance. The interaction of RIF with liposomes formed by 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) in different pH values (i.e., 5.0, 6.2 and 7.4) was investigated by several biophysical techniques. The RIF's membrane concentration was quantified by partition coefficient (Kp) using derivative spectrophotometry. To predict the drug's location across the membrane, fluorescence quenching studies were performed using liposomes labeled with two different fluorescence probes. The effect of the drug on the biophysical parameters of the membrane was carried out by dynamic light scattering (DLS), and small-angle X-ray scattering (SAXS). The overall results confirm that the interactions of RIF with membranes are pH-dependent, being much more pronounced at the acidic pH. A correlation between the effect of RIF on the biophysical properties of the membranes and the pH was found, which may be useful in the development of novel analogs with higher efficacy and fewer side effects, and also to understand the higher selectivity of RIF to the membranes of the infected cells, as well as its side effects.

journal_name

Int J Pharm

authors

Pinheiro M,Pisco S,Silva AS,Nunes C,Reis S

doi

10.1016/j.ijpharm.2014.03.005

subject

Has Abstract

pub_date

2014-05-15 00:00:00

pages

190-7

issue

1-2

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(14)00144-6

journal_volume

466

pub_type

杂志文章
  • Investigation of pluronic and PEG-PE micelles as carriers of meso-tetraphenyl porphine for oral administration.

    abstract::Meso-tetraphenyl porphine (mTPP) is a highly lipophilic, fluorescent porphyrin derivate and it is used as photosensitizer on the treatment of malign neoplasms. The aim of this study was to prepare mTPP loaded pluronic F127 and polyethylene glycol-distearoyl phosphatidylethanolamine (PEG(2000)-DSPE) micelles to evaluat...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2006.09.030

    authors: Sezgin Z,Yuksel N,Baykara T

    更新日期:2007-03-06 00:00:00

  • Docetaxel-carboxymethylcellulose nanoparticles display enhanced anti-tumor activity in murine models of castration-resistant prostate cancer.

    abstract::Docetaxel (DTX) remains the only effective drug for prolonging survival and improving quality of life of metastatic castration resistant prostate cancer (mCRPC) patients. Despite some clinical successes with DTX-based therapies, advent of cumulative toxicity and development of drug resistance limit its long-term clini...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.05.021

    authors: Hoang B,Ernsting MJ,Murakami M,Undzys E,Li SD

    更新日期:2014-08-25 00:00:00

  • Cathepsin K inhibitor-polymer conjugates: potential drugs for the treatment of osteoporosis and rheumatoid arthritis.

    abstract::The role of the newly discovered cysteine protease, cathepsin K, in osteoporosis and rheumatoid arthritis is reviewed. The current development of cathepsin K inhibitors and their targeted delivery using synthetic polymer carriers are discussed. Future challenges and possible strategies to improve these delivery system...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2003.03.003

    authors: Wang D,Li W,Pechar M,Kopecková P,Brömme D,Kopecek J

    更新日期:2004-06-11 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

  • Novel combination of non-invasive morphological and solid-state characterisation of drug-loaded core-shell electrospun fibres.

    abstract::In recent years, core-shell nanofibrous drug delivery systems have received increasing attention due to their ability to incorporate two or more active pharmaceutical ingredients (APIs) individually into the desired layer (either core or sheath) and thereby finely tune the release profiles of even incompatible drugs i...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119706

    authors: Kazsoki A,Farkas A,Balogh-Weiser D,Mancuso E,Sharma PK,Lamprou DA,Zelkó R

    更新日期:2020-09-25 00:00:00

  • Enhanced antioxidation via encapsulation of isooctyl p-methoxycinnamate with sodium deoxycholate-mediated liposome endocytosis.

    abstract::Isooctyl p-methoxycinnamate(OMC) is a commonly used chemical ultraviolet B sunscreen that suffers rapid degradation with current delivery systems following sun exposure. In this study, deoxycholate-mediated liposome (DOC-LS) endocytosis was employed to improve the antioxidation effects of OMC following topical adminis...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.10.010

    authors: Zhang Y,Shen L,Zhang K,Guo T,Zhao J,Li N,Feng N

    更新日期:2015-12-30 00:00:00

  • α-Glucosyl hesperidin induced an improvement in the bioavailability of pranlukast hemihydrate using high-pressure homogenization.

    abstract::The α-glucosyl hesperidin (Hsp-G)-induced improvement of both the dissolution and absorption properties of pranlukast hemihydrate (PLH) was achieved by means of a high-pressure homogenization (HPH) processing. The average particle size in the HPH-processed suspension was decreased significantly after 50 cycles of proc...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.03.017

    authors: Uchiyama H,Tozuka Y,Asamoto F,Takeuchi H

    更新日期:2011-05-30 00:00:00

  • Preparation and evaluation of agglomerated crystals by crystallo-co-agglomeration: an integrated approach of principal component analysis and Box-Behnken experimental design.

    abstract::Poor mechanical properties of crystalline drug particles require wet granulation technique for tablet production which is uneconomical, laborious, and tedious. The present investigation was aimed to improve flow and mechanical properties of racecadotril (RCD), a poorly water soluble antidiarrheal agent, by a crystallo...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.04.073

    authors: Garala KC,Patel JM,Dhingani AP,Dharamsi AT

    更新日期:2013-08-16 00:00:00

  • Effect of storage on microstructural changes of Carbopol polymers tracked by the combination of positron annihilation lifetime spectroscopy and FT-IR spectroscopy.

    abstract::Different types of Carbopols are frequently applied excipients of various dosage forms. Depending on the supramolecular structure, their water sorption behaviour could significantly differ. The purpose of the present study was to track the supramolecular changes of two types of Carbopol polymers (Carbopol 71G and Ultr...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.06.028

    authors: Szabó B,Süvegh K,Zelkó R

    更新日期:2011-09-15 00:00:00

  • Design of surface ligands for blood compatible gold nanoparticles: Effect of charge and binding energy.

    abstract::Gold nanoparticle (AuNP) interaction with the blood compartment as a function of their charge and the binding energy of their surface ligand was explored. Citrate, polyallylamine and cysteamine stabilized AuNP along with dihydrolipoic acid and polyethylene glycol capped AuNP were synthesized and fully characterized. T...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119244

    authors: Beurton J,Lavalle P,Pallotta A,Chaigneau T,Clarot I,Boudier A

    更新日期:2020-04-30 00:00:00

  • Fabrication and in vivo evaluation of ligand appended paclitaxel and artemether loaded lipid nanoparticulate systems for the treatment of NSCLC: A nanoparticle assisted combination oncotherapy.

    abstract::The aim of present study was to develop folate appended PEGylated solid lipid nanoparticles(SLNs) of paclitaxel(FPS) and artemether(FAS). The SLNs were prepared by employing high pressure homogenization technique. The results of MTT assays revealed better cytotoxicity of FPS when given in combination with FAS on human...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119386

    authors: Khatri H,Chokshi N,Rawal S,Patel BM,Badanthadka M,Patel MM

    更新日期:2020-06-15 00:00:00

  • Determination of promethazine hydrochloride and its preparations by highly accurate nephelometric titration.

    abstract::A highly accurate nephelometric titration for the determination of promethazine hydrochloride and its preparations was presented. The titration operating conditions were studied and the solubility product constant of promethazine tetraphenylboron precipitation was determined. The result of the titration is comparable ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.05.043

    authors: Zhang Q,Zhan X,Li C,Lin T,Li L,Yin X,He N,Shi Y

    更新日期:2005-09-30 00:00:00

  • Design of PEI-conjugated bio-reducible polymer for efficient gene delivery.

    abstract::The poly(cystaminebis(acrylamide)-diaminohexane) (poly(CBA-DAH)) was designed previously as a bio-reducible efficient gene delivery carrier. However, the high weight ratio required to form the polyplexes between poly(CBA-DAH) with pDNA is still a problem that needs to be addressed. To solve this problem and increase t...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.04.051

    authors: Nam JP,Kim S,Kim SW

    更新日期:2018-07-10 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

  • DPI formulations for high dose applications - Challenges and opportunities.

    abstract::This opinion piece gives reasons for high dose DPI applications, points out challenges and shows opportunities and possible solutions for high dose DPI. This piece of work shall set the stage for more in-depth reviews of state of the art and research papers addressing the challenges of high dose DPI which shall be inc...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2018.06.038

    authors: Scherließ R,Etschmann C

    更新日期:2018-09-05 00:00:00

  • Validation of fluid bed granulation utilizing artificial neural network.

    abstract::Three innovative components (an annular gap spray system, a booster bottom and an outlet filter) have been developed by Innojet Technologies to improve fluid bed technology and to reduce the common interference factors (clogging of nozzles and outlet filters, spray loss, spray drying and fluidized bed heterogeneity). ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.07.051

    authors: Behzadi SS,Klocker J,Hüttlin H,Wolschann P,Viernstein H

    更新日期:2005-03-03 00:00:00

  • Reformulation of etoposide with solubility-enhancing rubusoside.

    abstract::Etoposide (ETO), a widely used anti-cancer drug, is constrained by its low aqueous solubility and by side effects from both the drug and its solubilizing excipients. In this study, a recently discovered natural solubilizer rubusoside (RUB) was used to achieve the solubilization of ETO. Dynamic light scattering and fre...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.06.013

    authors: Zhang F,Koh GY,Hollingsworth J,Russo PS,Stout RW,Liu Z

    更新日期:2012-09-15 00:00:00

  • Influence of in vitro release methods on assessment of tobramycin ophthalmic ointments.

    abstract::The current investigation was carried out to identify appropriate parameters for measuring the in vitro release of tobramycin (TOB) ophthalmic ointments and to evaluate the feasibility of in vitro release testing methods to assess the product performance. Drug release was assessed using USP dissolution apparatus IV an...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119938

    authors: Patere S,Newman B,Wang Y,Choi S,Mekjaruskul C,Jay M,Lu X

    更新日期:2020-11-30 00:00:00

  • Development of a novel human stratum corneum model, as a tool in the optimization of drug formulations.

    abstract::Transdermal delivery represents a very attractive administration route that provides various advantages over other methods of administration, including enhanced patient compliance via non-invasive, painless and simple application and reduced side effects. Thereby, the research on suitable drugs for this route continue...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.118571

    authors: Shakel Z,Nunes C,Costa Lima SA,Reis S

    更新日期:2019-10-05 00:00:00

  • Delivery of salmon calcitonin using a microneedle patch.

    abstract::Peptides and polypeptides have important pharmacological properties but only a limited number have been exploited as therapeutics because of problems related to their delivery. Most of these drugs require a parenteral delivery system which introduces the problems of pain, possible infection, and expertise required to ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.11.046

    authors: Tas C,Mansoor S,Kalluri H,Zarnitsyn VG,Choi SO,Banga AK,Prausnitz MR

    更新日期:2012-02-28 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

  • Differences in physical chemistry and dissolution rate of solid particle aerosols from solution pressurised inhalers.

    abstract::Solution composition alters the dynamics of beclomethasone diproprionate (BDP) particle formation from droplets emitted by pressurised metered dose inhalers (pMDIs). The hypothesis that differences in inhaler solutions result in different solid particle physical chemistry was tested using a suite of complementary calo...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.01.033

    authors: Buttini F,Miozzi M,Balducci AG,Royall PG,Brambilla G,Colombo P,Bettini R,Forbes B

    更新日期:2014-04-25 00:00:00

  • Novel self-floating tablet for enhanced oral bioavailability of metformin based on cellulose.

    abstract::Metformin has several problems such as low bioavailability, short half-life, and narrow absorption window, sustained and site-specific drug delivery system is required. Floating drug delivery systems are very useful to achieve these purposes. However, conventional floating systems have several limitations; lag time, a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.120113

    authors: Wook Huh H,Na YG,Kang H,Kim M,Han M,Mai Anh Pham T,Lee H,Baek JS,Lee HK,Cho CW

    更新日期:2021-01-05 00:00:00

  • Ex vivo skin permeation and retention studies on chitosan-ibuprofen-gellan ternary nanogel prepared by in situ ionic gelation technique--a tool for controlled transdermal delivery of ibuprofen.

    abstract::The chemical potentials of drug-polymer electrostatic interaction have been utilized to develop a novel ternary chitosan-ibuprofen-gellan nanogel as controlled transdermal delivery tool for ibuprofen. The ternary nanogels were prepared by a combination of electrostatic nanoassembly and ionic gelation techniques. The e...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.05.030

    authors: Abioye AO,Issah S,Kola-Mustapha AT

    更新日期:2015-07-25 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

  • Application of DoE approach in the development of mini-capsules, based on biopolymers and manuka honey polar fraction, as powder formulation for the treatment of skin ulcers.

    abstract::The aim of the present work was the development of a powder formulation for the delivery of manuka honey (MH) bioactive components in the treatment of chronic skin ulcers. In particular pectin (PEC)/chitosan glutamate (CS)/hyaluronic acid (HA) mini-capsules were obtained by inverse ionotropic gelation in presence of c...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2016.10.050

    authors: Tenci M,Rossi S,Bonferoni MC,Sandri G,Mentori I,Boselli C,Cornaglia AI,Daglia M,Marchese A,Caramella C,Ferrari F

    更新日期:2017-01-10 00:00:00

  • Improved pH-dependent drug release and oral exposure of telmisartan, a poorly soluble drug through the formation of drug-aminoclay complex.

    abstract::Telmisartan (TEL) belongs to BCS class II (low solubility/high permeability) and exhibits the pH-dependent drug release. Since 3-aminopropyl functionalized magnesium phyllosilicate (aminoclay) can intercalate or adsorb the negatively charged molecules via the electrostatic interaction, TEL-aminoclay complex was synthe...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2014.05.009

    authors: Yang L,Shao Y,Han HK

    更新日期:2014-08-25 00:00:00

  • Release profiles and morphological characterization by atomic force microscopy and photon correlation spectroscopy of 99mTechnetium-fluconazole nanocapsules.

    abstract::Several classes of antifungal have been employed in candidiasis treatment, but patients with advanced immunodeficiency can present unsatisfactory results after therapy. In these cases, high doses of drugs or the use of multiple agents are sometimes used, and hence increasing the risk of serious side effects. Consideri...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2007.08.002

    authors: de Assis DN,Mosqueira VC,Vilela JM,Andrade MS,Cardoso VN

    更新日期:2008-02-12 00:00:00

  • Statistical optimisation of diclofenac sustained release pellets coated with polymethacrylic films.

    abstract::The objective of the present study was to evaluate three formulation parameters for the application of polymethacrylic films from aqueous dispersions in order to obtain multiparticulate sustained release of diclofenac sodium. Film coating of pellet cores was performed in a laboratory fluid bed apparatus. The chosen in...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(03)00061-9

    authors: Kramar A,Turk S,Vrecer F

    更新日期:2003-04-30 00:00:00

  • The influence of high shear mixing on ternary dry powder inhaler formulations.

    abstract::The blending process is a key step in the production of dry powder inhaler formulations, but only little is known about the influence of process parameters. This is especially true for high shear blending of ternary formulations. For this reason, this study aims to investigate the influence of high shear mixing proces...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.10.033

    authors: Hertel M,Schwarz E,Kobler M,Hauptstein S,Steckel H,Scherließ R

    更新日期:2017-12-20 00:00:00