Publications by authors named "G Lambiase"

The secretory capacity of Chinese hamster ovary (CHO) cells remains a fundamental bottleneck in the manufacturing of protein-based therapeutics. Unconventional biological drugs with complex structures and processing requirements are particularly problematic. Although engineered vector DNA elements can achieve rapid and high-level therapeutic protein production, a high metabolic and protein folding burden is imposed on the host cell.

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Films for coffee-pod packaging usually contain aluminium as an impermeable foil that is not recyclable and has to be discharged as waste. In this study, a recyclable polypropylene multilayer film is proposed as an alternative. The performance on the chemical composition of coffee was evaluated and compared to that of film containing aluminium (standard).

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Coffee pods and capsules require packaging that guarantees the optimal coffee preservation. The chemical composition of coffee can undergo quality decay phenomena during storage, especially in terms of lipidic and volatile components. Amongst coffee packaging, aluminum multilayer materials are particularly widely diffused.

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By employing Tsallis' extensive but non-additive δ-entropy, we formulate the first two laws of thermodynamics for gravitating systems. By invoking Carathéodory's principle, we pay particular attention to the integrating factor for the heat one-form. We show that the latter factorizes into the product of thermal and entropic parts, where the entropic part cannot be reduced to a constant, as is the case in conventional thermodynamics, due to the non-additive nature of Sδ.

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Article Synopsis
  • High-throughput screening in biopharmaceuticals cuts costs and speeds up drug development by enabling rapid selection of effective cell lines using small-scale cell culture systems like 24- and 96-deep-well plates.
  • The study focuses on analyzing protein aggregation, a critical factor affecting drug safety and effectiveness, by integrating automated purification and aggregation evaluation of therapeutic proteins expressed in these plates.
  • The new workflow allows for efficient screening of numerous clonal cell lines (384 in 32 hours) with minimal protein requirements, identifying and eliminating those with high aggregation levels early in the development process.
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