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Okay fair but how much of that 1.5 - 2mls of Yohimbine actually reaches the blood stream and/or fat cells? Where as with the inj version I would thinks this figure is close to 100%.ultimate thug i have been in contact with the guys about the product, it contains 20mg of yohimbine HCL per 4 squirts,that about the same as using 1.5-2.0mls of reverzine per shot, now,a bottle is only 20mls and u are getting a bottle for only slightly cheaper than sculpt,then u have to buy insulin needles at about R26 for 10,so u can see that the price isnt that high
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DJ wrote:
Okay fair but how much of that 1.5 - 2mls of Yohimbine actually reaches the blood stream and/or fat cells? Where as with the inj version I would thinks this figure is close to 100%.ultimate thug i have been in contact with the guys about the product, it contains 20mg of yohimbine HCL per 4 squirts,that about the same as using 1.5-2.0mls of reverzine per shot, now,a bottle is only 20mls and u are getting a bottle for only slightly cheaper than sculpt,then u have to buy insulin needles at about R26 for 10,so u can see that the price isnt that high
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vega5 wrote:
DJ wrote:
Okay fair but how much of that 1.5 - 2mls of Yohimbine actually reaches the blood stream and/or fat cells? Where as with the inj version I would thinks this figure is close to 100%.ultimate thug i have been in contact with the guys about the product, it contains 20mg of yohimbine HCL per 4 squirts,that about the same as using 1.5-2.0mls of reverzine per shot, now,a bottle is only 20mls and u are getting a bottle for only slightly cheaper than sculpt,then u have to buy insulin needles at about R26 for 10,so u can see that the price isnt that high
Yeah, that's a good point!
The biopharmaceutics of yohimbine (YO) and the pharmacokinetics of 10-hydroxy-yohimbine (10-OH-YO) and 11-hydroxy-yohimbine (11-OH-YO) were investigated in healthy subjects following i.v. (5 mg) and oral (8 mg) dosing. One subject was found as a slow hydroxylator of YO. The mean (+/-S.D.) oral absolute bioavailability of YO was 22.3+/-21. 5%. Total plasma clearance (CL) and renal clearance (CL(r)) of YO following i.v. dosing were 0.728+/-0.256 ml/min and 0.001+/-0.002 ml/min, respectively. Based on the steady-state volume of distribution (V(ss)), YO had a relatively low distribution (V(ss) = 32.2+/-12.1 l). The overall renal excretion of YO, 10-OH-YO and 11-OH-YO, expressed as percent of the dose of YO administered, were not different following i.v. and oral dosing, and were around 0.1, 0.2 and 14%, respectively. Following i.v. dosing of YO, the mean apparent terminal half-life of 11-OH-YO (347+/-63 min) was almost four times higher than that of YO (91.0+/-33.6 min) suggesting an elimination rate-limited kinetics for 11-OH-YO.
Pharmacokinetic profiles were determined in seven healthy young male subjects following single oral and intravenous doses of 10 mg of yohimbine hydrochloride. The drug was rapidly eliminated (t1/2 beta 0.58 h orally and t1/2 beta 0.68 h intravenously). Following intravenous administration the data fit a two-compartment pharmacokinetic model, with a very rapid distribution phase (t1/2a was approximately 6 min). Both the oral and the intravenous yohimbine clearance values were high but oral clearance values were much higher (mean 9.77 ml.min-1.kg-1 intravenous versus 55.9 ml.min-1.kg-1 oral). The oral bioavailability showed great variability, ranging from 7% to 87% (mean value was 33%). The incomplete oral bioavailability of yohimbine may reflect either incomplete absorption from the gastrointestinal tract or an hepatic first pass effect. Although yohimbine is rapidly absorbed when given orally, the bioavailability is quite variable and considerable individualization of dosing may be necessary when the drug is used orally for clinical indications.
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admin wrote:
vega5 wrote:
DJ wrote:
Okay fair but how much of that 1.5 - 2mls of Yohimbine actually reaches the blood stream and/or fat cells? Where as with the inj version I would thinks this figure is close to 100%.ultimate thug i have been in contact with the guys about the product, it contains 20mg of yohimbine HCL per 4 squirts,that about the same as using 1.5-2.0mls of reverzine per shot, now,a bottle is only 20mls and u are getting a bottle for only slightly cheaper than sculpt,then u have to buy insulin needles at about R26 for 10,so u can see that the price isnt that high
Yeah, that's a good point!The biopharmaceutics of yohimbine (YO) and the pharmacokinetics of 10-hydroxy-yohimbine (10-OH-YO) and 11-hydroxy-yohimbine (11-OH-YO) were investigated in healthy subjects following i.v. (5 mg) and oral (8 mg) dosing. One subject was found as a slow hydroxylator of YO. The mean (+/-S.D.) oral absolute bioavailability of YO was 22.3+/-21. 5%. Total plasma clearance (CL) and renal clearance (CL(r)) of YO following i.v. dosing were 0.728+/-0.256 ml/min and 0.001+/-0.002 ml/min, respectively. Based on the steady-state volume of distribution (V(ss)), YO had a relatively low distribution (V(ss) = 32.2+/-12.1 l). The overall renal excretion of YO, 10-OH-YO and 11-OH-YO, expressed as percent of the dose of YO administered, were not different following i.v. and oral dosing, and were around 0.1, 0.2 and 14%, respectively. Following i.v. dosing of YO, the mean apparent terminal half-life of 11-OH-YO (347+/-63 min) was almost four times higher than that of YO (91.0+/-33.6 min) suggesting an elimination rate-limited kinetics for 11-OH-YO.
Pharmacokinetic profiles were determined in seven healthy young male subjects following single oral and intravenous doses of 10 mg of yohimbine hydrochloride. The drug was rapidly eliminated (t1/2 beta 0.58 h orally and t1/2 beta 0.68 h intravenously). Following intravenous administration the data fit a two-compartment pharmacokinetic model, with a very rapid distribution phase (t1/2a was approximately 6 min). Both the oral and the intravenous yohimbine clearance values were high but oral clearance values were much higher (mean 9.77 ml.min-1.kg-1 intravenous versus 55.9 ml.min-1.kg-1 oral). The oral bioavailability showed great variability, ranging from 7% to 87% (mean value was 33%). The incomplete oral bioavailability of yohimbine may reflect either incomplete absorption from the gastrointestinal tract or an hepatic first pass effect. Although yohimbine is rapidly absorbed when given orally, the bioavailability is quite variable and considerable individualization of dosing may be necessary when the drug is used orally for clinical indications.
Seems that even the injectable and oral have a low bioavailability, so the transdermal can't be better... Should even be less.
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The fat on women's thighs is more difficult to mobilize due to increased alpha-2 adrenergic receptor activity induced by estrogen. Lipolysis can be initiated through adipocyte receptor stimulation (beta adrenergic) or inhibition (adenosine or alpha-2 adrenergic) or by inhibition of phosphodiesterase. Since many women desire regional thigh fat loss, a series of clinical trials were initiated using one thigh as a double-blinded control. Trial #1: Five overweight women had injections of isoproterenol at intervals around the thigh three times a week for 4 weeks with diet and walking. Trial #2: Five overweight woman had ointment containing forskolin, yohimbine and aminophylline applied to the thigh five times a week for 4 weeks after hypertonic warm soaks with a diet and walking. Trial #3: Eighteen overweight women were divided into three groups of six and trial #2 was repeated with each agent alone vs. placebo using forskolin, yohimbine or aminophylline in separate ointments. Trial #4: Thirty overweight women had 10% aminophylline ointment applied to the thigh five times a week for 6 weeks with diet and walking. Chemistry panel, theophylline level and patch testing were performed. Trial #5: Twelve women had trial #4 repeated with 2% aminophylline cream without a diet or walking. Trial #6: Trial #5 was repeated with 0.5% aminophylline cream. All trials except yohimbine ointment gave significantly more girth loss from the treated thigh (p < 0.05 to p < 0.001). Chemistry panel showed no toxicity. Theophylline was undetectable and patch testing was negative. We conclude that topical fat reduction for women's thighs can be achieved without diet or exercise.
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PMID: 8697059
The fat on women's thighs is more difficult to mobilize due to increased alpha-2 adrenergic receptor activity induced by estrogen. Lipolysis can be initiated through adipocyte receptor stimulation (beta adrenergic) or inhibition (adenosine or alpha-2 adrenergic) or by inhibition of phosphodiesterase. Since many women desire regional thigh fat loss, a series of clinical trials were initiated using one thigh as a double-blinded control. Trial #1: Five overweight women had injections of isoproterenol at intervals around the thigh three times a week for 4 weeks with diet and walking. Trial #2: Five overweight woman had ointment containing forskolin, yohimbine and aminophylline applied to the thigh five times a week for 4 weeks after hypertonic warm soaks with a diet and walking. Trial #3: Eighteen overweight women were divided into three groups of six and trial #2 was repeated with each agent alone vs. placebo using forskolin, yohimbine or aminophylline in separate ointments. Trial #4: Thirty overweight women had 10% aminophylline ointment applied to the thigh five times a week for 6 weeks with diet and walking. Chemistry panel, theophylline level and patch testing were performed. Trial #5: Twelve women had trial #4 repeated with 2% aminophylline cream without a diet or walking. Trial #6: Trial #5 was repeated with 0.5% aminophylline cream. All trials except yohimbine ointment gave significantly more girth loss from the treated thigh (p < 0.05 to p < 0.001). Chemistry panel showed no toxicity. Theophylline was undetectable and patch testing was negative. We conclude that topical fat reduction for women's thighs can be achieved without diet or exercise.
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DMSOmaybe the trial was not effective due to the transport system,The Sculpt Transport system might be a DSMO solution which would be more effective than any other ointment used to transport yohimbine through the skin.i will clarify later.
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Sculpt Gel wrote:
DMSOmaybe the trial was not effective due to the transport system,The Sculpt Transport system might be a DSMO solution which would be more effective than any other ointment used to transport yohimbine through the skin.i will clarify later.
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hahahahahaha always clowning around hey
guys i have just bought a bottle for my lady,i will slap some tan on her this weekend and take a photo of the areas she will be applying,she will be applying to the buttocks and abdomen twice a day,she works a full time job and doesnt diet or exercise so it will be a good way to judge!i will then take photos two weeks post and then 4 weeks post starting sculpt and will report back the results!!! (yes you will get to see my chicks ass)
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did my editing privilages get taken away admin?i was gonna edit the posts...
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