149 related articles for article (PubMed ID: 24523739)
1. Dissolution rate enhancement of clarithromycin using ternary ground mixtures: nanocrystal formation.
Shahbaziniaz M; Foroutan SM; Bolourchian N
Iran J Pharm Res; 2013; 12(4):587-98. PubMed ID: 24523739
[TBL] [Abstract][Full Text] [Related]
2. Preparation and physicochemical characterization of binary and ternary ground mixtures of carvedilol with PVP and SLS aimed to improve the drug dissolution.
Bolourchian N; Talamkhani Z; Nokhodchi A
Pharm Dev Technol; 2019 Nov; 24(9):1115-1124. PubMed ID: 31282827
[TBL] [Abstract][Full Text] [Related]
3. Formation, physical stability and in vitro antimalarial activity of dihydroartemisinin nanosuspensions obtained by co-grinding method.
Chingunpitak J; Puttipipatkhachorn S; Chavalitshewinkoon-Petmitr P; Tozuka Y; Moribe K; Yamamoto K
Drug Dev Ind Pharm; 2008 Mar; 34(3):314-22. PubMed ID: 18363147
[TBL] [Abstract][Full Text] [Related]
4. Novel ultra-cryo milling and co-grinding technique in liquid nitrogen to produce dissolution-enhanced nanoparticles for poorly water-soluble drugs.
Sugimoto S; Niwa T; Nakanishi Y; Danjo K
Chem Pharm Bull (Tokyo); 2012; 60(3):325-33. PubMed ID: 22382412
[TBL] [Abstract][Full Text] [Related]
5. Glucosamine HCl as a new carrier for improved dissolution behaviour: effect of grinding.
Al-Hamidi H; Edwards AA; Mohammad MA; Nokhodchi A
Colloids Surf B Biointerfaces; 2010 Nov; 81(1):96-109. PubMed ID: 20674291
[TBL] [Abstract][Full Text] [Related]
6. Investigation into physical-chemical variables affecting the manufacture and dissolution of wet-milled clarithromycin nanoparticles.
Shahbazi Niaz M; Traini D; Young PM; Ghadiri M; Rohanizadeh R
Pharm Dev Technol; 2014 Dec; 19(8):911-21. PubMed ID: 24093825
[TBL] [Abstract][Full Text] [Related]
7. Solid state and dissolution rate characterization of co-ground mixtures of nifedipine and hydrophilic carriers.
Friedrich H; Nada A; Bodmeier R
Drug Dev Ind Pharm; 2005 Sep; 31(8):719-28. PubMed ID: 16221606
[TBL] [Abstract][Full Text] [Related]
8. Effect of glucosamine HCl on dissolution and solid state behaviours of piroxicam upon milling.
Al-Hamidi H; Edwards AA; Douroumis D; Asare-Addo K; Nayebi AM; Reyhani-Rad S; Mahmoudi J; Nokhodchi A
Colloids Surf B Biointerfaces; 2013 Mar; 103():189-99. PubMed ID: 23201737
[TBL] [Abstract][Full Text] [Related]
9. Enhanced dissolution and bioavailability of raloxifene hydrochloride by co-grinding with different superdisintegrants.
Jagadish B; Yelchuri R; K B; Tangi H; Maroju S; Rao VU
Chem Pharm Bull (Tokyo); 2010 Mar; 58(3):293-300. PubMed ID: 20190431
[TBL] [Abstract][Full Text] [Related]
10. Antisolvent precipitation technique: A very promising approach to crystallize curcumin in presence of polyvinyl pyrrolidon for solubility and dissolution enhancement.
Sadeghi F; Ashofteh M; Homayouni A; Abbaspour M; Nokhodchi A; Garekani HA
Colloids Surf B Biointerfaces; 2016 Nov; 147():258-264. PubMed ID: 27518458
[TBL] [Abstract][Full Text] [Related]
11. Improvement of dissolution property of poorly water-soluble drug by novel dry coating method using planetary ball mill.
Sonoda R; Horibe M; Oshima T; Iwasaki T; Watano S
Chem Pharm Bull (Tokyo); 2008 Sep; 56(9):1243-7. PubMed ID: 18758094
[TBL] [Abstract][Full Text] [Related]
12. Dissolution enhancement and in vitro performance of clarithromycin nanocrystals produced by precipitation-lyophilization-homogenization method.
Morakul B; Suksiriworapong J; Chomnawang MT; Langguth P; Junyaprasert VB
Eur J Pharm Biopharm; 2014 Nov; 88(3):886-96. PubMed ID: 25201298
[TBL] [Abstract][Full Text] [Related]
13. Dissolution Kinetics of Meloxicam Formulations Co-Milled with Sodium Lauryl Sulfate.
Patera J; Němečková P; Zámostný P
Pharmaceutics; 2022 Oct; 14(10):. PubMed ID: 36297608
[TBL] [Abstract][Full Text] [Related]
14. Use of the co-grinding method to enhance the dissolution behavior of a poorly water-soluble drug: generation of solvent-free drug-polymer solid dispersions.
Yang C; Xu X; Wang J; An Z
Chem Pharm Bull (Tokyo); 2012; 60(7):837-45. PubMed ID: 22790815
[TBL] [Abstract][Full Text] [Related]
15. Design of PVP/VA S-630 based tadalafil solid dispersion to enhance the dissolution rate.
Choi JS; Park JS
Eur J Pharm Sci; 2017 Jan; 97():269-276. PubMed ID: 27919702
[TBL] [Abstract][Full Text] [Related]
16. Enhancement of the dissolution rate and gastrointestinal absorption of pranlukast as a model poorly water-soluble drug by grinding with gelatin.
Chono S; Takeda E; Seki T; Morimoto K
Int J Pharm; 2008 Jan; 347(1-2):71-8. PubMed ID: 17689212
[TBL] [Abstract][Full Text] [Related]
17. Effect of grinding with hydroxypropyl cellulose on the dissolution and particle size of a poorly water-soluble drug.
Yamada T; Saito N; Imai T; Otagiri M
Chem Pharm Bull (Tokyo); 1999 Sep; 47(9):1311-3. PubMed ID: 10517010
[TBL] [Abstract][Full Text] [Related]
18. Co-grinding with surfactants as a new approach to enhance in vitro dissolution of praziquantel.
Gaggero A; Jurišić Dukovski B; Radić I; Šagud I; Škorić I; Cinčić D; Jug M
J Pharm Biomed Anal; 2020 Sep; 189():113494. PubMed ID: 32745904
[TBL] [Abstract][Full Text] [Related]
19. Solid-state characterization and dissolution properties of meloxicam-moringa coagulant-PVP ternary solid dispersions.
Noolkar SB; Jadhav NR; Bhende SA; Killedar SG
AAPS PharmSciTech; 2013 Jun; 14(2):569-77. PubMed ID: 23483432
[TBL] [Abstract][Full Text] [Related]
20. Drug nanoparticle formation from drug/HPMC/SDS ternary ground mixtures.
Moribe K; Pongpeerapat A; Tozuka Y; Yamamoto K
Pharmazie; 2006 Feb; 61(2):97-101. PubMed ID: 16526554
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
