I finally started research on net through the pharmaceutical polymer data. Low and behold they have this *ucking polymer that reacts to hydrxoides to form a mass surrounding the drug so that the drug will not be assorbed until entering the intestine. Hydoxide is the OH- that comes through base disassociation ie: dissolving lye or sodium carbonate, sodium bicarbonate, (and on and on) in an aquaeous solution (water). Minimal amounts of polymer is even needed, as in parts per billion. The easy solution is to use another polymer to pull the shit polymer out of solution
Thanks to WayUpNorth for the quote and research above....
In a step reaction mechanism, monomers can react with any nearby monomer. In contrast to chain polymerization, no special activation is needed to allow a monomer to react. Frequently these reactions are copolymerizations, where two types of monomer are present and each reacts only with the other (and not with monomers like itself) This type of polymerization is also called condensation polymerization because water is often liberated when the polymer bonds form. Example reactions include
Polyester formation: The monomers are diols and diacids. The acid groups react with the alcohol groups to form ester linkages.
from
http://islnotes.cps.msu.edu/trp/back/cls_poly.html (http://islnotes.cps.msu.edu/trp/back/cls_poly.html)