Impact of various nonionic surfactants on self-nanoemulsification efficiency of two grades of Capryol (Capryol-90 and Capryol-PGMC)
The aim of present study was to investigate the impact of various combinations of nonionic
surfactants on self-nanoemulsification efficiency of two grades of Capryol (Capryol-90 and …
surfactants on self-nanoemulsification efficiency of two grades of Capryol (Capryol-90 and …
Formulation and in vitro evaluation of self-nanoemulsifying liquisolid tablets of furosemide
Self-nanoemulsifying drug delivery systems (SNEDDS) were used to enhance the
dissolution rate of furosemide as a model for class IV drugs and the system was solidified …
dissolution rate of furosemide as a model for class IV drugs and the system was solidified …
Self-nanoemulsifying drug-delivery system and solidified self-nanoemulsifying drug-delivery system
Self-nanoemulsifying drug-delivery systems (SNEDDSs) and solidified self-nanoemulsifying
drug-delivery systems (S-SNEDDSs) are considered promising drug carriers to enhance the …
drug-delivery systems (S-SNEDDSs) are considered promising drug carriers to enhance the …
Impact of solid carriers and spray drying on pre/post-compression properties, dissolution rate and bioavailability of solid self-nanoemulsifying drug delivery system …
In the present study, different solid self-nanoemulsifying drug delivery system (S-SNEDDS)
was formulated by using porous hydrophilic and hydrophobic carriers to improve the …
was formulated by using porous hydrophilic and hydrophobic carriers to improve the …
Formulation by design of felodipine loaded liquid and solid self nanoemulsifying drug delivery systems using Box–Behnken design
Objective: To design and develop liquid and solid self-nanoemulsifying drug delivery
systems (SNEDDS and S-SNEDDS) of felodipine (FLD) using Box–Behnken design (BBD) …
systems (SNEDDS and S-SNEDDS) of felodipine (FLD) using Box–Behnken design (BBD) …
Solid self-nanoemulsifying systems of olmesartan medoxomil: Formulation development, micromeritic characterization, in vitro and in vivo evaluation
S Beg, OP Katare, S Saini, B Garg, RK Khurana… - Powder technology, 2016 - Elsevier
The current studies entail development and evaluation of solid self-nanoemulsifying drug
delivery systems (S-SNEDDS) employing porous carriers for enhancing the oral …
delivery systems (S-SNEDDS) employing porous carriers for enhancing the oral …
New solid self-microemulsifying systems to enhance dissolution rate of poorly water soluble drugs
Context: An adequate drug dissolution behavior is essential for the therapeutic effectiveness
of all solid dosage forms. Objective: To develop a new solid self-micro-emulsifying drug …
of all solid dosage forms. Objective: To develop a new solid self-micro-emulsifying drug …
Preparation and evaluation of self-nanoemulsifying tablets of carvedilol
The purpose of this study was to combine the advantages of self-nanoemulsifying drug
delivery systems and tablets as a conventional dosage form emphasizing the excipients' …
delivery systems and tablets as a conventional dosage form emphasizing the excipients' …
Self‐Nanoemulsifying Powder of Isotretinoin: Preparation and Characterization
H Chavda, J Patel, G Chavada, S Dave… - Journal of Powder …, 2013 - Wiley Online Library
In the present investigation an attempt was made to enhance the solubility and dissolution of
poorly soluble drug, isotretinoin, by formulating self‐nanoemulsifying drug delivery system …
poorly soluble drug, isotretinoin, by formulating self‐nanoemulsifying drug delivery system …
Design and optimization of a new self-nanoemulsifying drug delivery system
L Wang, J Dong, J Chen, J Eastoe, X Li - Journal of colloid and interface …, 2009 - Elsevier
To improve the dissolution rate of ibuprofen, a model poorly water soluble drug, self-
nanoemulsifying drug delivery systems (SNEDDS) were developed. Various surfactants and …
nanoemulsifying drug delivery systems (SNEDDS) were developed. Various surfactants and …