Polyoxyethylene membranes

In the first example, procaine penicillin, an aqueous vehicle containing the soluble components (such as lecithin, sodium citrate, povidone, and polyoxyethylene sorbitan monooleate) is filtered through a 0.22 pm membrane filter, heat sterilized, and transferred into a presterilized mixing-filling tank. The sterile antibiotic powder, which has previously been produced by freeze-drying, sterile crystallization, or spray-drying, is aseptically added to the sterile solution while mixing. After all tests have been completed on the bulk formulation, it is aseptically filled. 

Detergent must not be very expensive Detergent should be readily removable after treating membrane fraction Detergent must not interfere with assays such as lipids, protein colorimetric determinations and enzymatic activity many of the nonionic detergents contain high phosphate levels that interfere with certain lipid analyses and certain of the polyoxyethylene derivatives affect protein colorimetric and enzyme assays... 

Interactions of Nonionic Polyoxyethylene Alkyl and Aryl Ethers with Membranes and Other Biological Systems... 

It has been recognised for some time (see for example reference 1), that surfactants can increase the rate and extent of transport of solute molecules through biological membranes by fluidisation of the membrane. It is only recently, however, that sufficient work has been carried out to allow some analysis of structure-action relationships. In this overview an attempt is made, by reference to our own work and to work in the literature, to define those structural features in polyoxyethylene alkyl and aryl ethers which give rise to biological activity, especially as it is manifested in interactions with biomembranes and subsequent increase in the transport of drug molecules. 

The difficulty with HLB as an index of physicochemical properties is that it is not a unique value, as the data of Zaslavsky et al. (1) on the haemolytic activity of three alkyl mercaptan polyoxyethylene derivatives clearly show in Table 1. Nevertheless data on promotion of the absorption of drugs by series of nonionic surfactants, when plotted as a function of HLB do show patterns of behaviour which can assist in pin-pointing the necessary lipophilicity required for optimal biological activity. It is evident however, that structural specificity plays a part in interactions of nonionic surfactants with biomembranes as shown in Table 1. It is reasonable to assume that membranes with different lipophilicities will"require" surfactants of different HLB to achieve penetration and fluidization one of the difficulties in discerning this optimal value of HLB resides in the problems of analysis of data in the literature. For example, Hirai et al. (8 ) examined the effect of a large series of alkyl polyoxyethylene ethers (C4,C0, Cj2 and C 2 series) on the absorption of insulin through the nasal mucosa of rats. Some results are shown in Table II. 

More recently, Carafa et al. showed that niosomes could be obtained from polyoxyethylene sorbitan monolaurate-cholesterol in aqueous environment. These authors investigated the delivery of lidocaine HC1 and lidocaine base from vesicles through silicone membrane and nude mice skin [44]. It was found that only the charged molecule (loading pH 5.5) could be encapsulated within the vesicles ( 30%). This behavior was explained by the entrapment ability of the hydrophilic moiety within the aqueous core of the vesicles. The lipophilic unionized form of lidocaine (loading pH 8.6) remained unattached. The amount of lidocaine permeated through nude mice skin from these niosomes was similar to liposomes and only about twofold greater than from a micellar system. 

Polyhedral niosomes were found to be thermoresponsive Fig. 7 (a). Above 35 °C, there was an increase in the release of CF from these niosomes even though the polyhedral shape was preserved until these vesicles were heated to 50 °C. Solulan C24-free polyhedral niosomes do not exhibit this thermoresponsive behavior [160] due to a decrease in the interaction of the polyoxyethylene compound solulan C24 with water at this temperature (due to decreased hydrogen bonding) as identified by viscometry [161]. This observed thermoresponsive behavior was used to design a reversible thermoresponsive controlled release system Fig. 7 (b). Thermoresponsive liposomal systems which rely on the changing membrane permeability, when the system transfers from the gel state (La) to the liquid crystal state (L 3) [162], are not reversible. This is not unex-... 

Surfactants Sodium lauryl sulfate, saponin, polyoxyethylene-9-lauryl ether, polyoxyethylene-20-lauryl ether, alkylmaltosides such as tetradecylmaltoside, dodecylmaltoside, and decylmaltoside Membrane disruption... 

The presence of 0.1%(v/v) of polyoxyethylene sorbitan monolaurate (Tween-20) in all buffers during the processing of the membrane asasts the prevention of nonspecific binding. 

Most synthetic methods for the generation of peptide libraries have been derived from various multiple parallel peptide synthesis techniques developed since 1984.bs-i l Consequently, the sohd supports used for hbrary synthesis are essentially the same as those used for multiple peptide synthesis. Standard divinylbenzene cross-linked polystyrene resins are typically used for hbraries that are cleaved from the resin and screened in solution.P Polyoxyethylene-grafted polystyrene resins,f l or acrylamide-polyoxyethylene copolymers, P on the other hand, are the sohd supports of choice for the synthesis of resin-bound peptide hbraries screened in sohd-phase binding assays.P Such resins are compatible with both organic solvents used for peptide synthesis, as well as aqueous buffers used in the bioassays. Various segmental supports previously employed for multiple peptide syntheses have also been utilized for the synthesis of peptide libraries, including polypropylene pins, PI cotton,t cellulose membrane,and glass shdes.P ... 

Tsubouchi and Yoshikawa [79] are concerned with pervaporation separation of benzene/cyclohexane mixtures using membranes based on polyamide/polyether block copolymers. It has been established that the separation factor increases with the increase in the polyamide component containing polar amide groups capable of forming hydrogen bonds e.g., the 1 1 block copolymer of polyamide 12 and polyoxyethylene has the benzene/cyclohexane separation factor /3p = 2.8 and the flux 2 = 300 g/m h a more rigid 3 1 polyamide 12/polyoxyethylene block copolymer has a much higher separation factor )8p = 5.0 and 2 = 80 g/m h. 

Sugiura, M., Effect of polyoxyethylene-n-alkyl ethers on carrier mediated transport of lanthanide ions through cehulose triacetate membranes. Sep. Sci. Tech., 1992, 27 269-276. 

In view of their solubilizing effects and also their potential to change membrane permeability, surfactants have been considered as absorption enhancers, again mostly in animals. Polyoxyethylene ethers have been shown to enhance gastric or rectal absorption of linco-mycin, penicillin, cephalosporins, and fosfomycin in rats and rabbits. In rats, colonic absorption of interferon-alpha is increased from 3 to 8% by polyoxyethylene esters of oleic acid and oleic acid glycerides. 

Surfactants Sodium lauryl sulfate Polyoxyethylene oxide-9 ethers Solubilization of proteins/peptides Perturbation of membrane layers Extraction of membrane proteins and lipids... 

Sawicki W, Janlckl S. Influence of polyoxyethylene-lO-oleylether on in vitro verapamil hydrochloride penetration through mucous membrane from model buccal drug formulation. STP Pharma Sci 1998 8(2) 107-111. 

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