Abstract: This invention relates to a novel method of drug targeting which comprises covalently binding a drug to a lipid carrier. This composition has the unique ability to both enhance the rate at which an antineoplastic or antiviral drug crosses the plasma membrane, and to direct the drug within the cell to specific organelles. The versatility of these conjugates may be further enhanced by including a spacer group between the drug and the lipid which may act to modulate drug release at the target site.

Abstract: L-gulono gamma lactone is made in a one-step process by the simultaneous hydrolysis and catalytic reduction with hydrogen in acid medium of polyglucuronic acid or a lower alkyl glucuronoside. A use statement--L gulono gamma lactone can be converted chemically or biologically to L-ascorbic acid (vitamin C).

Abstract: Dialdehyde cellulose is produced by reacting cellulose in aqueous medium with meta periodate ion used in a molar ratio of from 1.2 to 12 moles of meta periodate ion per mole of cellulose at a temperature of from 36.degree. to 60.degree. C. and a pH of between 2 and the conversion pH of water soluble meta periodate to water insoluble para periodate, and separating the dialdehyde cellulose product from the reaction mixture.

Abstract: Di- and tricarboxy celluloses are hydrolyzed with sulfurous acid in an aqueous medium to a mixture of erythronic acid and glyoxylic acid, in the case of dicarboxy cellulose; to a mixture of meso tartaric acid and glyoxylic acid in the case of tricarboxy cellulose; and to a mixture of these three products, in the case of a feedstock comprising a mixture of di- and tricarboxy celluloses.

Abstract: Mixtures of oxalic, meso tartaric, glyoxylic and erythronic acids derived particularly from the oxidation of cellulose derivatives are separated from aqueous solutions in which they are contained and from each other by stepwise precipitation with calcium ion at controlled pH. The oxalic acid is precipitated as calcium oxalate at a pH of 0.9 to 2.0; the tartaric acid as calcium meso tartrate at a pH of 2.8 to 4.4; and the glyoxylic acid, as calcium glyoxylate at a pH of 4.5 to 5.4. After each precipitation the water insoluble precipitate is separated from the aqueous mixture in which it is contained. The relatively soluble erythronic acid remains in solution as a free acid, or in the form of its calcium salt.