liposome analysis and sorting

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Does anybody out there know - and would be willing to share - anything
about flow analysis and sorting of artificially made liposomes? We have
just started a project to make immunoliposomes (tagged with an antibody,
to be preferentially taken up by specific tissues) of specific size (to
standardize the internal volume). Any suggestion will be greatly appreciated!

Thanks in advance,

Jacek

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Dr. Jacek M. Witkowski MD, PhD
Flow Cytometry Lab,
Department of Histology and Immunology
Medical University of Gdansk, Poland
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CD ROM Vol 2 was produced by staff at the Purdue University Cytometry Laboratories and distributed free of charge as an educational service to the cytometry community. If you have any comments please direct them to Dr. J. Paul Robinson, Professor & Director, PUCL, Purdue University, West Lafayette, IN 47907. Phone:(317) 494-0757; FAX (317) 494-0517; Web http://www.cyto.purdue.edu EMAIL robinson@flowcyt.cyto.purdue.edu