solid dispersion

CONCLUSION: Ethylcellulose is suitable to be sustained release solid dispersion excipient.

Setting up the topic by that, solid dispersion was studied to innovate on its dosage-form.

Methods Etodolac solid dispersion was prepared with PEG as carrier by solvent-fusion method and identified by differential thermal analysis.

Objective To prepare vinpocetine( VIN ) solid dispersion(SD) and improve the dissolution profile of vinpocetine.

METHODS Using the orthogonal design, it was prepared nifedipine solid dispersion by melting method, then filling into hard capsule.

Results: The results showed that solid dispersion give much higher improvement than physical mixture in the dissolution rate.

OBJECTIVE To prepare vinpocetine solid dispersion and improve the dissolution of vinpocetine.

Conclusion The sample of Galactosylglucose and Gliclazide can form solid dispersion by high speed grinding.

Conclusion: Raman spectrometry which is fast, direct and non-damaged is an ideal method in identifying solid dispersion.

Result: solid dispersion method can effective promoting the dissolution.

Objective: To improve the solubility and in vitro dissolution of isosorbide dinitrate(ISDN) solid dispersion.

RESULTS: X-ray diffraction methods showed that FD was numerous crystals existing in the solid dispersion.

abstract: OBJECTIVE To improve the solubility of candesartan by using solid dispersion(SD) technology.

Objective: A rapid release capsule of NMP was developed using solid dispersion techniques.

Objective To prepare apigenin (AP) solid dispersion and measure its dissolution in vitro.

Preparation methods had little effect on the dissolution rates of daidzein solid dispersion.

Results: Acetaminophen combined with PEG 6000 by hydrogen bond, and acetaminophen was dispersed in solid dispersion.

OBJECTIVE The solid dispersion method was adopted to enhance the dissolution rate of nifedipine (NFDP) which is a poorly water-soluble drug.

Objective To optimize the method of preparing Dragon's blood solid dispersion .

Results: Enrofloxacin and PEG6 000 were linked by hydrogen bond, and enrofloxacin was dispersed in solid dispersion.

AIM Preparing the solid dispersion of anethole trithione so as to increase its solubility and dissolution rate.

Method: Bomeolum Syntheticum and PEG 6000 mixing preparative solid dispersion and packed capsules, toxicity was tested.

Objective: To study bioavailability of baicalein and its coprecipitate, solid dispersion.

OBJECTIVE To study the formation and solubilization mechanism of cefuroxime axetil solid dispersion.

Preparation and Thermodynamics of Moclobemide-Polyvinylpyrrolidone Solid Dispersion

Studies on improvement of dissolution and modification of dissolution rate of nisoldipine with binary solid dispersion

Study on the preparation and its dissolution rate of acemetacin solid dispersion

Preparation of cryptotanshinone solid dispersion and its properties

Application of Physicochemical Characterization Methods and Release Model in the Release Mechanism and Stability of Solid Dispersion

Preparation of solid dispersion hemin and evaluation of its dispersing character

Preparation of solid dispersion tablets of nitrendipine and its dissolution in vitro

Study on preparation and physical-chemical characteristics of indomethacin solid dispersion

Application of Solid Dispersion Technology in Sustained and Controlled Release Preparations

Preparation of the Solid Dispersion-Effervescent Tablets of Praziquantel

Preliminary Investigation on Interphase Mass Transfer in Agitated Liquid-Liquid-Solid Dispersion

Effects of carrier and surfactant on the dissolution rate of silybin in silymarin solid dispersion

Preparation and Dissolution Rate of Gliquidone Solid Dispersion

Studies on preparation and dissolution of the enteric solid dispersion of dipyridamole

Study on the solid dispersion of rosiglitazone maleate and its dissolution rate

Application of solid dispersion procedure in sustained-release agents compounding

Preparation of itraconazole solid dispersion with PVP and dissolution experiment in vitro

Effect of Illumination on In-vitro Dissolution Behavior of Nitrendipine Solid Dispersion Pellets

Preparation of Curcumin Solid Dispersion Systems and Their Dissolution Test in vitro

Preparation of Fenofibrate Solid Dispersion Tablets

Dissolution of nimodipine solid dispersion tablets

Preparation of tinidazole solid dispersion by orthogonal test

Interaction of Puerarin with Phospholipid in Solid Dispersion

Preparation of Nimodipine Solid Dispersion

Study on Stability of Nitrendipine Solid Dispersion Pellets

The study of Preparation of nimodipine solid dispersion and their dissolution

Preparation of Usolic Acid Solid Dispersion Capsule and Study on its Dissolution in vitro

Study on dissolution test method of Silybin Solid Dispersion Capsules

Studies on formation and solubilizing mechanism of oleanolic acid solid dispersion

Study on the preparation and in vitro evaluation of vinpocetine solid dispersion

Study on the preparation and in vitro evaluation of cyclosporine A solid dispersion

Preparation and in vivo Evaluation of Probucol Solid Dispersion

Progress of Preparation of Solid Dispersion

Stability of Solid Dispersion of Tanshinone

Preparation of Usolic Acid Solid Dispersion Systems and Study on Their Dissolution in Vitro

Advances of aging and resistance of aging of solid dispersion

Preparation and Analysis of Solid Dispersion Systems of Usolic Acid

Study on Solid Dispersion of Tanshinone