Lignocellulose represents a key sustainable source of biomass for transformation into biofuels and bio‐based products. Unfortunately, lignocellulosic biomass is highly recalcitrant to biotransformation, both microbial and enzymatic, which limits its use and prevents economically viable conversion into value‐added products. As a result, effective pretreatment strategies are necessary, which invariably involves high energy processing or results in the degradation of key components of lignocellulose. In this work, the ionic liquid, 1‐ethyl‐3‐methylimidazolium acetate ([Emim][CH₃COO]), was used as a pretreatment solvent to extract lignin from wood flour. The cellulose in the pretreated wood flour becomes far less crystalline without undergoing solubilization. When 40% of the lignin was removed, the cellulose crystallinity index dropped below 45, resulting in >90% of the cellulose in wood flour to be hydrolyzed by Trichoderma viride cellulase. [Emim] [CH₃COO] was easily reused, thereby resulting in a highly concentrated solution of chemically unmodified lignin, which may serve as a valuable source of a polyaromatic material as a value‐added product. Biotechnol. Bioeng. 2009;102: 1368–1376.

Effective pretreatment of lignocellulosic biomass is vital to its bioconversion to a usable liquid fuel. A growing body of work has focused on using room temperature ionic liquids (RTILs) to pretreat lignocellulose for subsequent fermentation. However, little is known about the physicochemical parameters of RTILs that promote effective pretreatment. In this work we examine the relationship between the Kamlet–Taft α, β, and π* solvent polarity parameters of different RTILs ([Emim][OAc], [Bmim][OAc], and [Bmim][MeSO₄]) and effective pretreatment of lignocellulosic biomass. We find the β parameter is an excellent predictor of pretreatment efficacy. Acetate containing RTILs (β > 1.0) remove >32% of lignin from maple wood flour and significantly reduce cellulose crystallinity, resulting in >65% glucose yields after 12 h cellulase hydrolysis. Pretreatment in [Bmim][MeSO₄] (β = 0.60) results in the removal of only 19% of the wood flour's lignin with no decrease in crystallinity, and no improvement in sugar yield over untreated wood flour. The addition of water and the dilution of the acetate anion with the methyl sulfate anion decrease the β value and subsequently have a negative impact on lignin extraction, cellulose crystallinity, and sugar yields.

We have developed a miniaturized 3D cell-culture array (the Data Analysis Toxicology Assay Chip or DataChip) for high-throughput toxicity screening of drug candidates and their cytochrome P450-generated metabolites. The DataChip consists of human cells encapsulated in collagen or alginate gels (as small as 20 nl) arrayed on a functionalized glass slide for spatially addressable screening against multiple compounds. A single DataChip containing 1,080 individual cell cultures, used in conjunction with the complementary human P450-containing microarray (the Metabolizing Enzyme Toxicology Assay Chip or MetaChip), simultaneously provided IC₅₀values for nine compounds and their metabolites from CYP1A2, CYP2D6, and CYP3A4 and a mixture of the three P450s designed to emulate the human liver. Similar responses were obtained with the DataChip and conventional 96-well plate assays, demonstrating that the near 2,000-fold miniaturization does not influence the cytotoxicity response. The DataChip may therefore enable toxicity analyses of drug candidates and their metabolites at throughputs compatible with the availability of compounds at early-stage drug discovery.