Caffeine Estradiol

Nicolazzo JA, Reed BL, Finnin BC (2004a) Assessment of the effects of sodium dodecyl sulfate on the buccal permeability of caffeine and estradiol. J Pharm Sci 93 431-440... 

Smoking cessation, with or without nicotine substitutes, may alter response to concomitant medication in ex-smokers. Smoking may affect alcohol, benzodiazepines, beta-adrenergic blockers, caffeine, clozapine, fluvoxamine, olanzapine, tacrine, theophylline, clorazepate, lidocaine (oral), estradiol, flecanide, imipramine, heparin, insulin, mexiletine, opioids, propranolol, catecholamines, and cortisol. 

CA149 Nagata, C., M. Kabuto, and H. Shimizu. CAl61 Association of coffee, green tea, and caffeine intakes with serum concentrations of estradiol and sex hormonebinding globulin in premenopausal Japanese women. Nutr Cancer 1998 CA162... 

P450 IA2 -fin women Inhibited by P-estradiol, progesterone, and OCs Caffeine, theophylline, demethylation of TCAs Fluvoxamine... 

Nicolazzo et al. [52] considered the use of the lipophilic skin penetration enhancers, octisalate and padimate (both used in sunscreens), in comparison to Azone on the buccal absorption of various drugs in vitro. They were found to have limited effect in enhancing the permeation of triamcinolone acetonide (although some increase in tissue uptake was proposed in some cases) relative to Azone, while reducing the penetration of estradiol and caffeine. One interesting report is that of the effect of capsaicin from capsicum, a commonly used food ingredient, which has been reported to enhance the permeability of sulfathiazole in human volunteers [53] presumably by a direct irritation effect on the mucosa. This raised an interesting issue of the effect of diet on oral mucosal permeability. 

A2 Phenacetin, theophylline, acetaminophen, warfarin, caffeine, cimetidine Aromatic amines, arylhydrocarbons, NNK,3 aflatoxin, estradiol Caffeine, [acetanilide, methoxyresorufin, ethoxyresorufin]... 

Mosbach and co-workers developed a method to prepare molecularly imprinted polymers by precipitation polymerization [24]. They started from a dilute, homogenous solution of the monomer methacrylic acid (MAA) and the crosslinker trimethylolpropane trimethacrylate (TRIM) or ethylene glycol dimethacrylate (EGDMA). The polymer formed in the presence of the template molecule 17/1-estradiol, theophylline, or caffeine contained a high proportion of discrete spheres of diameter less than a micron. Because the effect of coalescence becomes predominant with higher solid content of the reaction mixture, this approach is limited to solid contents of typically <2 wt%. 

Kaul L, Curry CL, Ahluwalia BS. Blood levels of ethynyl-estradiol, caffeine, aldosterone and desoxycorticosterone... 

The efflux transporter P-glycoprotein (P-gp) has been proposed as a potential therapeutic target for AD [439]. Approximately 10-35 % decrease in 125I-Ap(i 0) intracellular accumulation was observed in cells treated with rifampicin, dexamethasone, caffeine, verapamil, hyperforin, p-estradiol, and pentylenetetrazole, drugs known to induce P-gp expression [439],... 

On the other hand, SEPA (2-n-nonyl-l,3-dioxolane) has been shown to be a more versatile penetration enhancer in terms of its ease of formulation, chemical stability and its ability to enhance the skin penetration of a wide variety of compounds of varying physicochemical characteristics. Permeants that have been evaluated include indomethacin, ibuprofen, minoxidil, acyclovir, caffeine, econazole, papaverine, progesterone and estradiol. The degree of skin penetration enhancement using SEPA is dependent on the physicochemical characteristics of the permeant. For example, following application of indomethacin in a simple ethanol-propylene glycol vehicle to human skin in vitro, cumulative absorption over 24 h amounted to 0.7 percent of the applied dose. The addition of 2 percent SEPA to the vehicle increased the 24 h absorption value to 23 percent of the applied dose (Marty et al. 1989). Furthermore, in comparative studies between SEPA and Azone, SEPA was shown to be a more effective human skin permeation enhancer for indomethacin (Figure 14.6, Marty et al. 1989). 

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