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 candidates for cell replacement therapy and, in this regards, Parkinson's disease is of particular interest. It is one of the most prevalent neurodegenerative diseases caused by the loss of dopaminergic neurons in the Substantia nigra pars compacta. Pharmacological therapies are valuable but suffer from the progressive decline of efficacy as the disease progresses. Cell therapy application has emerged about two decades ago as a valid therapeutic alternative and recent advances in stem cell research suggest that pluripotent stem cell transplantation may be a promising approach to replace degenerated neurons in Parkinson's disease. Various sources of pluripotent stem cells (PSC) currently tested in animal models of Parkinson's disease have proven their efficacy in relieving symptoms and restoring damaged brain function. This review summarizes and discusses the important challenges that actually must be solved before the first studies of PSC transplantation can be undertaken into humans.

journal_name

Int J Pharm

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

doi

10.1016/j.ijpharm.2009.03.003

subject

Has Abstract

pub_date

2009-11-03 00:00:00

pages

113-21

issue

2

eissn

0378-5173

issn

1873-3476

pii

S0378-5173(09)00141-0

journal_volume

381

pub_type

杂志文章,评审
  • Fabrication of nanopatterned PLGA films of curcumin and TPGS for skin cancer.

    abstract::Squamous cell carcinoma treatment has limited therapeutic options and the incidence rate is increasing recently. In the present investigation, we developed poly(lactic-co-glycolic acid) (PLGA) nanopatterned films (NPFs) through poly dimethyl siloxane (PDMS) cast molding technique and explored its therapeutic efficacy ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119100

    authors: Malathi S,Pavithra PS,Sridevi S,Verma RS

    更新日期:2020-03-30 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

  • Microagglomeration of pulverized pharmaceutical powders using the Wurster process I. Preparation of highly drug-incorporated, subsieve-sized core particles for subsequent microencapsulation by film-coating.

    abstract::A novel agglomeration process of pulverized pharmaceutical powders into subsieve-sized agglomerates (microagglomeration) was designed for manufacturing highly drug-incorporated core particles for subsequent microencapsulation by film-coating. The microagglomeration of pulverized phenacetin powder, whose mass median di...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00006-x

    authors: Ichikawa H,Fukumori Y

    更新日期:1999-04-15 00:00:00

  • Formulation characteristics and in vitro release testing of cyclosporine ophthalmic ointments.

    abstract::The aim of the present study was to investigate the relationship between formulation/process variables versus the critical quality attributes (CQAs) of cyclosporine ophthalmic ointments and to explore the feasibility of using an in vitro approach to assess product sameness. A definitive screening design (DSD) was used...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.04.042

    authors: Dong Y,Qu H,Pavurala N,Wang J,Sekar V,Martinez MN,Fahmy R,Ashraf M,Cruz CN,Xu X

    更新日期:2018-06-10 00:00:00

  • Permeation of cyproterone acetate through pig skin from different vehicles with phospholipids.

    abstract::The permeation of cyproterone acetate (CPA) from Derma Membrane Structure (DMS) creams and liposomal formulations was investigated. Standard diffusion experiments with dermatomed porcine skin were performed. The cumulative CPA amount permeated of the DMS creams was between 2.9 and 6.8 microg/cm(2) within 48 h. By addi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(03)00180-7

    authors: Valenta C,Janisch M

    更新日期:2003-06-04 00:00:00

  • Synthesis, characterization of chitosan-tripolyphosphate conjugated chloroquine nanoparticle and its in vivo anti-malarial efficacy against rodent parasite: a dose and duration dependent approach.

    abstract::Various strategies to deliver antimalarials using nanocarriers have been evaluated. However, taking into account the peculiarities of malaria parasites, the focus is placed mainly polymer-based chitosan nanocarriers. Our purpose of the study is to develop chitosan-tripolyphosphate (CS-TPP) nanoparticles (NPs) conjugat...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2012.05.064

    authors: Tripathy S,Das S,Chakraborty SP,Sahu SK,Pramanik P,Roy S

    更新日期:2012-09-15 00:00:00

  • Advanced topical formulations (ATF).

    abstract::Topical formulations aim to target the skin for a variety of cosmetic, protective or therapeutic needs. Despite the use of creams and ointments over the millennia, the bioavailability of actives from topical preparations remains quite low, often not exceeding 1-2% of the applied dose. In this review we examine the rea...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2016.05.065

    authors: Hadgraft J,Lane ME

    更新日期:2016-11-30 00:00:00

  • Shape imposed by secondary structure of a polypeptide affects its free diffusion through liquid-filled pores.

    abstract::The purpose of the present study was to investigate the effect of secondary structure of three model polypeptides on their apparent permeability (P(app)) across a synthetic, microporous membrane. Poly-L-lysine (PL), poly-L-glutamate (PGlu), and poly-L-lysine-L-phenylalanine (1:1) (PLP) were selected because a solution...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(02)00320-4

    authors: Salamat-Miller N,Chittchang M,Mitra AK,Johnston TP

    更新日期:2002-09-05 00:00:00

  • Development and evaluation of a dimensionless mechanistic pan coating model for the prediction of coated tablet appearance.

    abstract::A mathematical, mechanistic tablet film-coating model has been developed for pharmaceutical pan coating systems based on the mechanisms of atomisation, tablet bed movement and droplet drying with the main purpose of predicting tablet appearance quality. Two dimensionless quantities were used to characterise the produc...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.05.060

    authors: Niblett D,Porter S,Reynolds G,Morgan T,Greenamoyer J,Hach R,Sido S,Karan K,Gabbott I

    更新日期:2017-08-07 00:00:00

  • A novel approach to oral iron delivery using ferrous sulphate loaded solid lipid nanoparticles.

    abstract::Iron (Fe) loaded solid lipid nanoparticles (SLN's) were formulated using stearic acid and iron absorption was evaluated in vitro using the cell line Caco-2 with intracellular ferritin formation as a marker of iron absorption. Iron loading was optimised at 1% Fe (w/w) lipid since an inverse relation was observed betwee...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.08.070

    authors: Zariwala MG,Elsaid N,Jackson TL,Corral López F,Farnaud S,Somavarapu S,Renshaw D

    更新日期:2013-11-18 00:00:00

  • Ni2+-mediated mitoxantrone encapsulation: improved efficacy of fast release formulation.

    abstract::Despite that in solution we cannot detect the interaction between Ni(2+) and mitoxantrone (MIT), Ni(2+) could mediate effective and stable MIT loading into large unilamellar vesicles (LUVs). The presence of nigericin had almost no influences on MIT encapsulation. However, in the presence of NH(3), the drug loading kin...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2008.09.045

    authors: Cui J,Li C,Wang L,Wang C,Yang H,Li Y,Zhang L,Zhang L,Guo W,Liang M

    更新日期:2009-02-23 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

  • Elaboration and evaluation of alginate foam scaffolds for soft tissue engineering.

    abstract::Controlling microarchitecture in polymer scaffolds is a priority in material design for soft tissue applications. This paper reports for the first time the elaboration of alginate foam-based scaffolds for mesenchymal stem cell (MSC) delivery and a comparative study of various surfactants on the final device performanc...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2017.02.060

    authors: Ceccaldi C,Bushkalova R,Cussac D,Duployer B,Tenailleau C,Bourin P,Parini A,Sallerin B,Girod Fullana S

    更新日期:2017-05-30 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

  • Enhanced anti-tumor and anti-metastasis therapy for triple negative breast cancer by CD44 receptor-targeted hybrid self-delivery micelles.

    abstract::Tumor growth and metastasis are multistep processes regulated by multiple signaling pathways. The successful treatment of cancer largely depends on the ability to inhibit metastatic process. Multiphase inhibition of metastasis is a promising approach. Here, we described a targeting delivery system which was constructe...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2020.119085

    authors: Yang Y,Long Y,Wang Y,Ren K,Li M,Zhang Z,Xiang B,He Q

    更新日期:2020-03-15 00:00:00

  • Characterization of nifedipine microparticles prepared by hot air coating technique.

    abstract::In the present work, the Hot Air Coating (HAC) technique was used to prepare microparticulate systems containing nifedipine. Binary mixtures constituting of nifedipine and cetearyl alcohol (CA) in different proportions (30:70, 50:50, 70:30) were studied: they were homogenized by mixing or milling before spray treatmen...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2005.01.010

    authors: Giovannelli L,Bellomi S,Pattarino F,Albertini B

    更新日期:2005-04-11 00:00:00

  • Comparative study of liposomes, ethosomes and transfersomes as carriers for enhancing the transdermal delivery of diflunisal: In vitro and in vivo evaluation.

    abstract::The current study aimed to develop an effective transdermal nanovesicular carrier of diflunisal that provides enhanced delivery through the skin. Two types of nanovesicles, ethosomes and transfersomes, were investigated and compared to conventional liposomes. Ethosomes with variable ethanol contents (10, 30 and 50%) a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2019.04.001

    authors: Abd El-Alim SH,Kassem AA,Basha M,Salama A

    更新日期:2019-05-30 00:00:00

  • Sterilization of implantable polymer-based medical devices: A review.

    abstract::This review article is focused on the sterilization techniques used for polymer-based implantable medical devices as well as the regulatory aspects governing sterile medical devices. Polymeric materials are increasingly used in implantable devices due to their biodegradable and biocompatible nature. Patients and medic...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章,评审

    doi:10.1016/j.ijpharm.2017.12.003

    authors: Tipnis NP,Burgess DJ

    更新日期:2018-06-15 00:00:00

  • Poly(acrylic acid) microspheres containing beta-cyclodextrin: loading and in vitro release of two dyes.

    abstract::Microspheres containing poly(acrylic acid) and beta-cyclodextrin or maltose were prepared by a w/o solvent evaporation technique. The dispersed aqueous phase contained poly(acrylic acid) (800 mg) and beta-cyclodextrin or maltose (0, 200 or 800 mg). Food-grade olive oil was the continuous phase. Microsphere particle si...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00190-8

    authors: Bibby DC,Davies NM,Tucker IG

    更新日期:1999-10-05 00:00:00

  • Granule size control and targeting in pulsed spray fluid bed granulation.

    abstract::The primary aim of the study was to investigate the effects of pulsed liquid feed on granule size. The secondary aim was to increase knowledge of this technique in granule size targeting. Pulsed liquid feed refers to the pump changing between on- and off-positions in sequences, called duty cycles. One duty cycle consi...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2009.04.041

    authors: Ehlers H,Liu A,Räikkönen H,Hatara J,Antikainen O,Airaksinen S,Heinämäki J,Lou H,Yliruusi J

    更新日期:2009-07-30 00:00:00

  • Formulating powder-device combinations for salmeterol xinafoate dry powder inhalers.

    abstract::Using salmeterol xinafoate (SX) as an active pharmaceutical ingredient, the effects of carrier lactose particle type, total lactose fines content and device resistance on dry powder inhaler performance were investigated in vitro. To mimic drug levels in commercial preparations, interactive mixtures containing 0.58% w/...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.05.028

    authors: Hassoun M,Ho S,Muddle J,Buttini F,Parry M,Hammond M,Forbes B

    更新日期:2015-07-25 00:00:00

  • Beta-cyclodextrin as a suitable solubilizing agent for in situ absorption study of poorly water-soluble drugs.

    abstract::To evaluate the intestinal permeability of poorly water-soluble compounds, it is of importance to completely dissolve them in a medium and to avoid precipitation during experiments. This study was undertaken to find an agent possessing a high-solubilizing capacity and exhibiting minimal modulating impact on membrane i...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.05.003

    authors: Oda M,Saitoh H,Kobayashi M,Aungst BJ

    更新日期:2004-08-06 00:00:00

  • Development of a controlled release formulation based on SLN and NLC for topical clotrimazole delivery.

    abstract::Solid lipid nanoparticles (SLN) and nanostructured lipid carriers (NLC) are colloidal carrier systems providing controlled release profiles for many substances. Clotrimazole-loaded SLN and NLC were prepared by the hot high pressure homogenization technique in order to evaluate the physical stability of these particles...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2004.02.032

    authors: Souto EB,Wissing SA,Barbosa CM,Müller RH

    更新日期:2004-06-18 00:00:00

  • Liposome surface charge influence on skin penetration behaviour.

    abstract::Vesicular systems have shown their ability to increase dermal and transdermal drug delivery. Their mechanism of drug transport into and through the skin has been investigated but remains a much debated question. Several researchers have outlined that drug penetration can be influenced by modifying the surface charge o...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.03.049

    authors: Gillet A,Compère P,Lecomte F,Hubert P,Ducat E,Evrard B,Piel G

    更新日期:2011-06-15 00:00:00

  • Powder bed 3D-printing of highly loaded drug delivery devices with hydroxypropyl cellulose as solid binder.

    abstract::3D-printing is a promising tool to pave the way to the widespread adaption of individualized medicine. Several printing techniques have been investigated and introduced to pharmaceutical research. Until now, only one 3D-printed medicine is approved on the US market. The medicine is manufactured via drop-on-powder depo...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2018.11.048

    authors: Infanger S,Haemmerli A,Iliev S,Baier A,Stoyanov E,Quodbach J

    更新日期:2019-01-30 00:00:00

  • Melatonin-loaded lecithin/chitosan nanoparticles: physicochemical characterisation and permeability through Caco-2 cell monolayers.

    abstract::In this study, the potential of lecithin/chitosan nanoparticles (NPs) as a mucoadhesive colloidal nanosystem for transmucosal delivery of melatonin was investigated. The size, zeta potential and melatonin loading of the lecithin/chitosan NPs were investigated as a function of lecithin type (Lipoid S45, S75 and S100) a...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2009.07.001

    authors: Hafner A,Lovrić J,Voinovich D,Filipović-Grcić J

    更新日期:2009-11-03 00:00:00

  • Development of self emulsifying lipid formulations of BCS class II drugs with low to medium lipophilicity.

    abstract::Lipid-based formulations can be effective drug delivery systems for poorly water-soluble chemical entities, provided they are designed with careful selection of the excipients, based on their role in the delivery system and in relation to drug properties. The primary factor leading to increased bioavailability is the ...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2015.09.009

    authors: Jannin V,Chevrier S,Michenaud M,Dumont C,Belotti S,Chavant Y,Demarne F

    更新日期:2015-11-10 00:00:00

  • Development of cyclosporine A-loaded dry-emulsion formulation using highly purified glycerol monooleate for safe inhalation therapy.

    abstract::The main objective of this study was to improve the safety and oxidative stability of glycerol monooleate (GMO)-based dry-emulsion (DE) formulation containing cyclosporine A (CsA) for inhalation therapy. GMO or highly purified GMO (hpGMO) was used as surfactant for the DE formulations (GMO/DE or hpGMO/DE), the toxicol...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2013.03.026

    authors: Sato H,Ogawa K,Kojo Y,Kawabata Y,Mizumoto T,Yamada S,Onoue S

    更新日期:2013-05-01 00:00:00

  • Modeling and simulation of compact strength due to particle bonding using a hybrid discrete-continuum approach.

    abstract::The compaction of powder beds into solid bodies occurs by virtue of the formation of inter-particle bonds. The mechanical strength of the compact depends on the type of bonding interaction, as well as, the inter-particle contact area created in the compression process. A hybrid quasi-continuum computational approach h...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/j.ijpharm.2011.06.006

    authors: Koynov A,Akseli I,Cuitiño AM

    更新日期:2011-10-14 00:00:00

  • Buccal permeation of [D-Ala(2), D-Leu(5)]enkephalin from liquid crystalline phases of glyceryl monooleate.

    abstract::The ex vivo buccal permeability of a [D-Ala(2), D-Leu(5)]enkephalin (DADLE) and glyceryl monooleate (GMO) was examined from the cubic and lamellar liquid crystalline phases of GMO and aqueous phosphate-buffered saline (pH 7.4, PBS) solution across excised porcine buccal mucosa mounted in a Franz cell. GMO was released...

    journal_title:International journal of pharmaceutics

    pub_type: 杂志文章

    doi:10.1016/s0378-5173(99)00357-9

    authors: Lee J,Kellaway IW

    更新日期:2000-02-15 00:00:00