Emulsions topical

Uses Lubricant for plastics o/w emulsifier for emulsions, topical applies. 

Crodacol C-90 Crodacol C-95 EP Stabilizer, emulsions topical emulsions... 

Microemulsions are treated in a separate section in this chapter. Unlike macro- or ordinary emulsions, microemulsions are generally thermodynamically stable. They constitute a distinctive type of phase, of structure unlike ordinary homogeneous bulk phases, and their study has been a source of fascination. Finally, aerosols are discussed briefly in this chapter, although the topic has major differences from those of emulsions and foams. 

There is a great deal more that could be said about emulsion polymerization or, for that matter, about free-radical polymerization in general. We shall conclude our discussion of the free-radical aspect of chain-growth polymerization at this point, however. This is not the end of chain-growth polymerization, however. There are four additional topics to be considered ... 

Sorbitan sesquioleate emulsions of petrolatum and wax are used as ointment vehicles in skin treatment. In topical appHcations, the inclusion of both sorbitan fatty esters and their poly(oxyethylene) derivatives modifies the rate of release and promotes the absorption of antibiotics, antiseptics, local anesthetics, vasoconstrictors, and other medications from suppositories, ointments, and lotions. Poly(oxyethylene(20)) sorbitan monooleate, also known as Polysorbate 80 (USP 23), has been used to promote absorption of ingested fats from the intestine (245). 

Retinyl Palmitate Topical 0.5-5% Emulsions Cosmetic agents ... 

Topical Formulations. Topical formulations by their very nature are usually multicomponent, and it is not surprising that neural networks have been applied to deal with this complexity. The first work was performed on hydrogel formulations containing anti-inflammatory drugs in Japan in 1997 [57], followed up by further studies in 1999 [58] and in 2001 [59]. Lipophilic semisolid emulsion systems have been studied in Slovenia [60, 61] and transdermal delivery formulations of melatonin in Florida [62]. In all cases, the superiority of neural networks over conventional statistics has been reported. 

Altvater, M., Rietz, R., Neubeet, R., Micromixer based formation of emulsions and creams for pharmaceutical applications, in Proceedings of the 4th International Conference on Microreaction Technology, IMRET 4, pp. 467 77 (5-9 March 2000), AIChE Topical Conf Proc., Atlanta, USA. 

The determination and analysis of sensory properties plays an important role in the development of new consumer products. Particularly in the food industry sensory analysis has become an indispensable tool in research, development, marketing and quality control. The discipline of sensory analysis covers a wide spectrum of subjects physiology of sensory perception, psychology of human behaviour, flavour chemistry, physics of emulsion break-up and flavour release, testing methodology, consumer research, statistical data analysis. Not all of these aspects are of direct interest for the chemometrician. In this chapter we will cover a few topics in the analysis of sensory data. General introductory books are e.g. Refs. [1-3]. 

Rheo-NMR [86] methods have been shown to be well-suited to emulsion rheology studies [28] and could be combined with any of the topics described above. The combination of structural and rheological measurements is a promising area for further research. 

Regardless of the cause, the mainstay of treatment for dry eye is artificial tears. Artificial tears augment the tear film topically and provide relief. If a patient uses artificial tears more than four times daily, recommend a preservative-free formulation. Preservative-free formulations are also appropriate if the patient develops an allergy to ophthalmic preservatives. Artificial tears are available in gel, ointment, and emulsion forms that provide a longer duration of relief and may allow for less frequent instillation. Ointment use is appropriate at bedtime.30... 

Anti-inflammatory agents may be used in conjunction with artificial tears. The only approved agent is cyclosporine emulsion. Administered topically, it is thought to act as a partial immuno-modulator suppressing ocular inflammation, but the exact mechanism is unknown. Cyclosporine emulsion increases tear production in some patients. Fifteen minutes should elapse after instillation of cyclosporine before artificial tears are instilled.31 Use of topical corticosteroids for short periods (e.g., 2 weeks) may suppress inflammation and ocular irritation symptoms. No topical corticosteroid is approved for this indication, however.30... 

The stability of suspensions, emulsions, creams, and ointments is dealt with in other chapters. The unique characteristics of solid-state decomposition processes have been described in reviews by D. C. Monkhouse [79,80] and in the monograph on drug stability by J. T. Carstensen [81]. Baitalow et al. have applied an unconventional approach to the kinetic analysis of solid-state reactions [82], The recently published monograph on solid-state chemistry of drugs also treats this topic in great detail [83],... 

Of all these formulations, it is the diverse semisolids that stand out as being uniquely topical. Semisolid systems fulfill a special topical need as they cling to the surface of the skin to which they are applied, generally until being washed off or worn off. In contrast, fluid systems have poor substantivity and readily streak and run off the desired area. Similarly, powders have poor staying properties. Importantly, the fundamental physicochemical characteristics of solutions, liquid emulsions and suspensions, and powders are independent of their route of application, and are discussed adequately elsewhere in this text and need not be reconsidered. This is not to say the compositions of such systems cannot be uniquely topical, for there are chemicals that can be safely applied to the... 

The types of microorganisms found in various products are Pseudomonas species, including Pseudomonas aeruginosa, Salmonella, species, Staphylococcus aureus, and Escherichia coli. The USP and other pharmacopoeias recommend certain classes of products to be tested for specified microbial contaminants, e.g., natural plant, animal, and some mineral products for the absence of Salmonella species, suspensions for the absence of E. coli, and topically administered products for the absence of P. aeruginosa and S. aureus. Emulsions are especially susceptible to contamination by fungi and yeasts. Consumer use may also result in the introduction of microorganisms. For aqueous-based products, it is therefore mandatory to include a preservative in the formulation in order to provide further assurance that the product retains its pharmaceutically acceptable characteristics until it is used by the patient. 

Youenang Piemi, M.P., Korner, D., Benita, S. and Marty, J.P. (1999) Positively and negatively charged submicron emulsions for enhanced topical delivery of antifungal drugs. Journal of Controlled Release, 58, 177-187. 

Creams are semisolid preparations meant for external application as emollients or as topical medications. They are semisolid emulsions of either the oil-in-water or the water-in-oil type. 

I, too, was caught up in the wave of enthusiasm for this new science which had the lofty goal of relating the properties of materials to their molecular structure, and, in the end, to "tailor-making molecules for specific properties. Since one of the big developments at that time was the newly-started synthetic rubber programs of the American and Canadian governments, I chose the topic of the emulsion copolymerization of butadiene-styrene as the subject of my doctoral dissertation. 

C. B. Lalor, G. L. Flynn, and N. Weiner. Formulation factors affecting release of drug from topical formulations. I. Effect of emulsion type upon in vitro delivery of ethyl p-aminobenzoate. J. Pharm. Sci. 83 1525-1528 (1994). 

Topical emulsion 2.5 mg estradiol hemihydrate/g (Rx) Estrasorb (Novavax)... 

Moderate to severe vasomotor symptoms associated with menopause - Use the lowest effective dose and for the shortest duration consistent with treatment goals and risks for the individual women. Periodically reevaluate patients as clinically appropriate (eg, at 3-month to 6-month intervals) to determine if treatment is still necessary. The single approved dose of estradiol topical emulsion is 3.48 g/day. The lowest effective dose for this indication has not been determined. 

Various types of PFC-based gels and gel-emulsions have been reported [5,66,67]. They may find applications in topical drug delivery, wound healing, and implantable drug depots and as low-friction, gas-permeant, repellent protective-barrier creams against toxic or aggressive media, and in cosmetics. 

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