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1.
Acta Pharmaceutica Sinica ; (12): 1667-1672, 2017.
Article in Chinese | WPRIM | ID: wpr-779774

ABSTRACT

As a new carrier of intercellular information, the exosomes is widely regarded as a natural drug carrier for its extensive distribution, non-immunity and targeting in human body. Chinese herbal drugs act at multiple targets and through different pathways in the prevention and treatment of diseases, but the preparation is relatively simple, there is a low solubility in the effective ingredients and low bioavailability, which limit the efficacy of the medicine. Using the new drug delivery approach of the exosomes, it is better to deliver the effective components to target cells. In this review, we reviewed the biological characteristics of exosomes and its application as a carrier of Chinese herbal drugs.

2.
Chinese Pharmaceutical Journal ; (24): 814-818, 2017.
Article in Chinese | WPRIM | ID: wpr-858702

ABSTRACT

In recent years, nanoparticle as drug carriers have been widely used in the pharmaceutical field. For some poorly soluble drugs or drugs with strong toxicity and side effects, the design of different nano drug carriers can help achieve improved solubility and targeted therapy. The nano targeted drug delivery system can deliver drug specifically to the target sites and realize controlled release of drugs, thereby increasing the bioavailability and efficacy of drugs and reducing the toxicity and side effects. In this paper, the recent progress in studies on the design of nanoparticles, their biological effects, and their application in the field of medicine are reviewed.

3.
Article in English | IMSEAR | ID: sea-176908

ABSTRACT

This study explored the effect of nano-crystalline cellulose (NCC) on Meloxicam (MX) solid dispersion (SD) prepared by co-grinding technique compared to micro-crystalline cellulose (MCC) in presence of lactose. MX-tablets were prepared by direct compression of different co-ground SDs or physical mixtures. The solubility, dissolution, SEM and DSC of different preparations were studied. Flow-through cell apparatus (FTC) was used to study the dissolution of MX from tablets at pH 7.4. Generally, the results revealed that increasing NCC loadings showed a direct increase in both the solubility and dissolution of MX. MCC did not improve either the solubility or the dissolution of MX in the physical mixture, while, co-grinding dramatically decreased the dissolution rate of MX. It was interesting to find that grinding of MX-powder alone or in a mixture with lactose highly increased MX solubility and dissolution. SEM as well as DSC were found to be very good tools, without a single exception, to describe the observed solubility and dissolution of MX in these proposed preparations. SEM-images showed the particle size reduction upon grinding or co-grinding techniques. While DSC-data proved that the crystalline structure of MX has been changed to an amorphous state.

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