S. Keith Nixon

Micellisation and gelation of diblock copolymers of ethylene oxide and propylene oxide in aqueous solution, the effect of P-block length

The aqueous solution properties of five diblock copolymers prepared by sequential anionic copolymerisation (i.e. E102P37, E104P52, E92P55, E104P60 and E98P73 where E denotes oxyethylene and P denotes oxypropylene) were studied across a wide range of concentration. The techniques used to study micellisation and micellar properties in dilute solution were static and dynamic light scattering, surface tension, and eluent gel-permeation chromatography. The gelation of concentrated solutions was also investigated. As expected, the critical micelle concentration (CMC) was lowered and the association number of the micelles was increased by an increase in P-block length. In contrast, the critical gel concentration was unchanged, consistent with the constant E-block length leading to micelles with essentially identical E-block fringes. Comparison of the CMCs of the diblock copolymers with those of triblock EmPnEm copolymers with the same P-block length shows the diblock copolymers to micellise more efficiently. A similar comparison of the CMCs of the diblock copolymers with those of EmBn copolymer (B denotes oxybutylene) shows the hydrophobicity of a P unit to be one-sixth that of a B unit. The possibility is explored of correlating the limiting association number of a spherical micelle with the hydrophobe block length of its constituent copolymer. Of the five copolymers, only dilute solutions of E98P73 were predominantly micellar at both room temperature and body temperature, and this copolymer must be a prime candidate in any consideration of the potential application of EmPn copolymers in the solubilisation and controlled release of drugs.

Self-association properties of oxyethylene/oxypropylene/oxyethylene triblock copolymer F88

Abstract Critical micelle temperatures (cmT) of triblock copolymer F88 (nominally E102P39E102), where E = oxyethylene and P = oxypropylene in aqueous solution were determined by light scattering and eluent GPC (aqueous solvent). Two samples originating from different suppliers (BASF Inc. and ICI plc) were investigated. The overall formulae of the two samples (checked by NMR) were essentially identical, but their GPC curves (THF solvent) differed significantly. Comparison of the cmTs obtained, including published values from a dye solubilization method, showed good agreement between techniques but poor agreement between samples i.e. differences of 10–15 °C across a range of concentrations.

Solubilisation capacity of Brij surfactants

The aim of this study was to investigate the potential of selected Brij non-ionic surfactants for enhancing the solubility of poorly water-soluble drugs. Griseofulvin was selected as a model drug candidate enabling comparisons to be made with the solubilisation capacities of other poly(ethylene oxide)-based copolymers. UV/Vis and (1)H NMR spectroscopies were used to quantify the enhancement of solubility of griseofulvin in 1 wt% aqueous micellar solutions of Brij 78 (C(18)H(37)E(20)), Brij 98 (C(18)H(35)E(20)) and Brij 700 (C(18)H(37)E(100)) (where E represents the OCH(2)CH(2) unit of the poly(ethylene oxide) chain) at 25, 37 and 40 °C. Solubilisation capacities (S(cp) expressed as mg griseofulvin per g Brij) were similar for Brij 78 and 98 (range 6-11 mg g(-1)) but lower for Brij 700 (3-4 mg g(-1)) as would be expected for the surfactant with the higher ethylene oxide content. The drug loading capacity of micelles of Brij 78 was higher than many di- and triblock copolymers with hydrophilic E-blocks specifically designed for enhancement of drug solubility.

Solubilisation of drugs in micellar solutions of diblock copolymers of ethylene oxide and styrene oxide

The solubilisation of two poorly soluble drugs, furosemide and nabumetone, in micellar solutions of diblock copolymers of ethylene oxide and styrene oxide has been studied at 25 and 37 degrees C and solubilisation capacities compared with published values for griseofulvin and docetaxel. Solubilisation in the micelle core, corrected for the different proportions of poly(styrene oxide) in the copolymers, was similar for all four drugs. The highest solubilisation capacities were found for a copolymer with worm-like micelles.