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     Abou dou Akambi (adiss) New member Username: adiss Post Number: 1 Registered: 5-2007 |
Hello. I am working on some liposome. I just joined the forum. My spectrometer is in the range from 0.8-2.2 micrometers wavelength. I am using some lipoflow with some essentials phospholipids(EPL). Other ingredients are soy lecithin, water and natural alcohol Interested in liposome spectrum, I dissolved a certain amount of lipoflow with solution of D2O. A)After getting the spectra of pure D2O and ethyl alcohol, I substracted them from the spectrum of solution of (D2O + Lipoflow-forte(liposome)) but did not substract the one of soy lecithin and water. I was thinking that may be the portion of the water can be neglected as they only mentioned that there is 12 % of natural alcohol as ingredient. For EPL we have 900mg amount per serving teaspoon.This is like a dietary B) Neglecting the ingredients as the percentage was not given, I substrated the spectra of solution of(D2O + Lipoflow-forte(liposome)) from the one of solution of pure D2O. The spectrum of liposome i am expecting is different in both cases. The one in A seems to me be the flipped it over of the spectrum of the alcohol when I look at the absorbance. The one in B showing couple main peaks. I don't know if I am heading in the right direction for the spectra I am looking for to be interpreted later and which one might be the right one. Any comments would be appreciated. Thank you. Regards, Akambi ------------------------------------------------- This is below the attachement code
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