Overcoming clofazimine intrinsic toxicity: statistical modelling and characterization of solid lipid nanoparticles.

about

Overcoming clofazimine intrinsic toxicity: statistical modelling and characterization of solid lipid nanoparticles.

Item

http://www.wikidata.org/entity/Q50048230

description

2018 nî lūn-bûn

@nan

2018年の論文

@ja

2018年学术文章

@wuu

2018年学术文章

@zh

2018年学术文章

@zh-cn

2018年学术文章

@zh-hans

2018年学术文章

@zh-my

2018年学术文章

@zh-sg

2018年學術文章

@yue

2018年學術文章

@zh-hant

name

Overcoming clofazimine intrins ...... of solid lipid nanoparticles.

@en

Overcoming clofazimine intrins ...... of solid lipid nanoparticles.

@nl

type

Item

label

Overcoming clofazimine intrins ...... of solid lipid nanoparticles.

@en

Overcoming clofazimine intrins ...... of solid lipid nanoparticles.

@nl

prefLabel

Overcoming clofazimine intrins ...... of solid lipid nanoparticles.

@en

Overcoming clofazimine intrins ...... of solid lipid nanoparticles.

@nl

P1476

Overcoming clofazimine intrins ...... n of solid lipid nanoparticles

@en

P2093

Alexandre C C Vieira

http://www.w3.org/2001/XMLSchema#string

P2860

Phagocytosed Clofazimine Biocrystals Can Modulate Innate Immune Signaling by Inhibiting TNFα and Boosting IL-1RA Secretion

Clofazimine: a review of its medical uses and mechanisms of action

Macrophages sequester clofazimine in an intracellular liquid crystal-like supramolecular organization

Preparation of a clofazimine nanosuspension for intravenous use and evaluation of its therapeutic efficacy in murine Mycobacterium avium infection.

Complexation of clofazimine by macrocyclic cucurbit[7]uril reduced its cardiotoxicity without affecting the antimycobacterial efficacy.

Nanocarrier for poorly water-soluble anticancer drugs--barriers of translation and solutions.

Physico-chemical stability of colloidal lipid particles.

Design and statistical modeling of mannose-decorated dapsone-containing nanoparticles as a strategy of targeting intestinal M-cells.

Antibiotic-free nanotherapeutics: ultra-small, mucus-penetrating solid lipid nanoparticles enhance the pulmonary delivery and anti-virulence efficacy of novel quorum sensing inhibitors.

The use of solid lipid nanoparticles for sustained drug release.

P31

scholarly article

P356

10.1098/RSIF.2017.0932

http://www.w3.org/2001/XMLSchema#string

P433

139

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

P577

2018-02-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

29436513

http://www.w3.org/2001/XMLSchema#string

P921

Amar

P932

5832736

http://www.w3.org/2001/XMLSchema#string