Entrapment of bioactive compounds within native albumin beads: III. Evaluation of parameters affecting drug release

MT Sheu, TD Sokoloski - PDA Journal of Pharmaceutical Science …, 1986 - journal.pda.org
A simple and easily controlled method for preparing microbeads has been developed using
aw/o emulsion technique. Under constant process variables (temperature, stirring, etc.), the …

[PDF][PDF] Entrapment of bioactive compounds within native albumin beads: II. Effects of rate and extent of crosslinking on microbead properties

MT Sheu, MA Moustafa, TD Sokoloski - J. Parenter. Sci. Technol., 1986 - researchgate.net
The rate of crosslinking ofserum albumin is affected by several parameters such as pH,
buffer concentration, and the ratio of serum albumin to glutaraldehyde concentration …

Albumin microspheres: effect of process variables on size distribution and in vitro release

BP Reddy, AK Dorle, DR Krishna - Drug Development and …, 1990 - Taylor & Francis
Albumin microspheres used as target drug delivery systems were prepared from egg
albumin by polymerization technique using glutaral dehyde as the cross linking agent. The …

Entrapment of bioactive compounds within native albumin beads

GP Royer, TK Lee, TD Sokoloski - PDA Journal of Pharmaceutical …, 1983 - journal.pda.org
To prepare an injectable delivery device for prolonged release and targeting of drugs is the
goal of many researchers. Ideally the poly mer matrix would be nonantigenic …

Potential use of albumin microspheres as a drug delivery system. I. Preparation and in vitro release of steroids

DJ Burgess, SS Davis, E Tomlinson - International journal of pharmaceutics, 1987 - Elsevier
Albumin microspheres were prepared by two different stabilization processes: chemical
denaturation and heat denaturation. The extent of stabilization was characterized by the …

Albumin microspheres as a drug delivery system: relation among turbidity ratio, degree of cross-linking, and drug release

OP Rubino, R Kowalsky, J Swarbrick - Pharmaceutical research, 1993 - Springer
The degree of cross-linking of albumin microspheres, with and without drug, was assessed
using turbidity measurements carried out in the presence of water and the protein …

Albumin microspheres. II. Effect of stabilization temperature on the release of adriamycin

PK Gupta, CT Hung, DG Perrier - International journal of pharmaceutics, 1986 - Elsevier
The effect of stabilization temperature on the rate of release of adriamycin from bovine
serum albumin (BSA) microspheres has been evaluated: Microspheres were prepared at …

Influence of stabilization temperature on the entrapment of adriamycin in albumin microspheres

PK Gupta, JM Gallo, CT Hung… - Drug Development and …, 1987 - Taylor & Francis
Adriamycin associated bovine serum albumin (BSA) microspheres have been prepared by
the method involving emulsion and suspension technology. Stabilization of the carrier matrix …

Preparation of hydrophilic albumin microspheres using polymeric dispersing agents

WE Longo, H Iwata, TA Lindheimer… - Journal of pharmaceutical …, 1982 - Elsevier
A new method for preparing glutaraldehyde cross-linked human serum albumin
microspheres has been developed. Important aspects of this method include addition of …

Albumin microspheres. IV. Effect of protein concentration and stabilization time on the release rate of adriamycin

PK Gupta, FC Lam, CT Hung - International journal of pharmaceutics, 1989 - Elsevier
The effects of protein concentration and heat-stabilization time at 120° C on the release rate
of adriamycin from microspheres have been investigated. The albumin concentration and …