Simple salts are known to influence the cloud point temperature of the aqueous solution of thermoresponsive compounds, such as poly-(N-isopropylacrylamide), PNIPAM. The effect of one series of anions (six potassium salts) and two series of cations (five alkali-metal hydroxides and chlorides, respectively) on the cloud point temperature of PNIPAM oligomers is investigated. All salts with the exception of low (<0.5 M) concentrations of KI are found to lower the cloud point temperature; the relationship between the temperature and the concentration of the added salt tends to be linear. The intensity of the effect of a given salt corresponds to its position in the Hoffmeister series. However, while the anions differ significantly in force, the cations-with the exception of Li + -show little difference in this regard. The observed effects are interpreted based on the structure making/structure breaking potential of the involved ions as evidenced by their viscosity B coefficients. While a relationship could be established for the anions this is less obvious for the cations. Moreover, while the structure breaking ability of the I --anion to some extent explains its salting in ability at low concentrations, it does not account for the linear salting out effect observed at higher concentrations. The second attempt to interpret the results is based on the solvophobic theory, i.e., takes the contribution of both electrostatic and hydrophobic interactions into account. Thermodynamic data on the phase separation obtained through differential scanning calorimetry are used to calculate the unitary free Gibbs energy as a function of the molal salt concentration.

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Recent advances in DNA-based medicine (gene therapy, genetic vaccination) have intensified the necessity for pharmaceutical-grade plasmid DNA purification at comparatively large scales. In this contribution triple-helix affinity precipitation is introduced for this purpose. A short, single-stranded oligonucleotide sequence (namely (CTT)(7)), which is capable of recognizing a complementary sequence in the double-stranded target (plasmid) DNA, is linked to a thermoresponsive N-isopropylacrylamide oligomer to form a so-called affinity macroligand (AML). At 4 degrees C, i.e., below its critical solution temperature, the AML binds specifically to the target molecule in solution; by raising the temperature to 40 degrees C, i.e., beyond the critical solution temperature of the AML, the complex can be precipitated quantitatively. After redissolution of the complex at lower temperature, the target DNA can be released by a pH shift to slightly alkaline conditions (pH 9.0). Yields of highly pure (plasmid) DNA were routinely between 70% and 90%. Non-specific co- precipitation of either the target molecule by the non-activated AML precursor or of contaminants by the AML were below 7% and presumably due to physical entrapment of these molecules in the wet precipitate. Ligand efficiencies were at least 1 order of magnitude higher than in triple-helix affinity chromatography.

The influence of small alkylamines with increasing carbon chain length (≤5) on the temperature‐induced precipitation of two N‐alkylacrylamide oligomers, poly‐N‐isopropylacrylamide [PNIPAAm; weight‐average molecular weight (Mw ) = 1600 g/mol] and poly‐N,N‐diethylacrylamide (PDEAAm; Mw = 4000 g/mol), from an aqueous solution was investigated. The alkylamines in question were too small to form micelles in the classical sense but were capable of premicellar aggregation. PNIPAAm was prepared by radical polymerization in the presence of a chain‐transfer agent and, therefore, carried a carboxylic acid end group. The structure was heterotactic. PDEAAm was prepared by anionic polymerization and, therefore, carried a butyl end group. The structure was predominately isotactic. The solubility of the oligomers was investigated by cloud‐point measurements and differential scanning calorimetry. In addition, pyrene was used as a fluorescent polarity probe. Alkylamines up to C2 depressed the lower critical solution temperature (LCST) of PNIPAAm, whereas higher alkylamines first depressed the LCST and at higher concentrations elevated it. The LCST minimum showed a clear dependence on the alkyl chain length and structure. For PDEAAm, only pentylamine addition resulted in an LCST minimum. Otherwise, the LCST was raised. When the critical self‐association concentration (CSAC) of the alkylamines in water was compared to the critical association concentration (CAC) in aqueous oligomer solutions, PDEAAm, but not PNIPAAm, stabilized mixed aggregates (CAC < CSAC). The transition enthalpy of PNIPAAm decreased with an increasing alkylamine concentration and became 0 above the CAC. For PDEAAm, no transition endotherm could be recorded above an alkylamine concentration of 0.1 M. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 4218–4229, 2000