RESUMO
In many cancers early intervention involves surgical resection of small localised tumour masses. Inadequate resection leads to recurrence whereas overzealous treatment can lead to organ damage. This work describes production of a HER2 targeting antibody Fab fragment dual conjugated to achieve both real time near-infrared fluorescent imaging and photodynamic therapy. The use of fluorescence emission from a NIR-dye could be used to guide resection of tumour bulk, for example during endoscopic diagnosis for oesophago-gastric adenocarcinoma, this would then be followed by activation of the photodynamic therapeutic agent to destroy untreated localised areas of cancer infiltration and tumour infiltrated lymph nodes. This theranostic agent was prepared from the Fab fragment of trastuzumab initially by functional disulfide re-bridging and site-specific click reaction of a NIR-dye. This was followed by further reaction with a novel pre-activated form of the photosensitiser chlorin e6 with the exposed fragments' lysine residues. Specific binding of the theranostic agent was observed in vitro with a HER2 positive cell line and cellular near-infrared fluorescence was observed with flow cytometry. Specific photo-activity of the conjugates when exposed to laser light was observed with HER2 positive but not HER2 negative cell lines in vitro, this selectivity was not seen with the unconjugated drug. This theranostic agent demonstrates that two different photo-active functions can be coupled to the same antibody fragment with little interference to their independent activities.
Assuntos
Antineoplásicos Imunológicos/farmacologia , Neoplasias/tratamento farmacológico , Fotoquimioterapia , Fármacos Fotossensibilizantes/farmacologia , Receptor ErbB-2/antagonistas & inibidores , Nanomedicina Teranóstica , Trastuzumab/farmacologia , Antineoplásicos Imunológicos/síntese química , Antineoplásicos Imunológicos/química , Proliferação de Células/efeitos dos fármacos , Sobrevivência Celular/efeitos dos fármacos , Relação Dose-Resposta a Droga , Ensaios de Seleção de Medicamentos Antitumorais , Humanos , Neoplasias/metabolismo , Neoplasias/patologia , Fármacos Fotossensibilizantes/síntese química , Fármacos Fotossensibilizantes/química , Receptor ErbB-2/metabolismo , Relação Estrutura-Atividade , Trastuzumab/química , Células Tumorais CultivadasRESUMO
Temperature is an important food preservation factor, affecting microbial growth. Secondary predictive models can be used for describing the impact of this factor on microbial growth. In other words, the microbial behavior can be described in a dynamic environment with the use of a primary and secondary model. Two models for describing the effect of temperature on the microbial growth rate are the cardinal temperature model with inflection (CTMI) (Rosso et al., 1993) and its adapted version (aCTMI) (Le Marc et al., 2002). Although Escherichia coli is commonly modeled using CTMI, there are indications that aCTMI may be more appropriate (Van Derlinden and Van Impe, 2012a). For clarifying this, the method of Optimal experiment design for model discrimination (OED/MD) will be used in this work (Donckels et al., 2009; Schwaab et al., 2008). Results from an in silico study point out the required direction. Whereas the results of the in vivo study give a more realistic answer to the research question. Finally, discrimination unravelled the appropriate model for the needed use.
RESUMO
In the field of predictive microbiology, mathematical models play an important role for describing microbial growth, survival and inactivation. Often different models are available for describing the microbial dynamics in a similar way. However, the model that describes the system in the best way is desired. Optimal experimental design for model discrimination (OED-MD) is an efficient tool for discriminating among rival models. In this work the T12-criterion proposed by Atkinson and Fedorov (1975) [1] and applied efficiently by Ucinski and Bogacka (2005) [2] and the Schwaab-approach proposed by Schwaab et al. (2008) [3] and Donckels et al. (2009) [4] will be applied for discriminating among rival models for the microbial growth rate as a function of temperature. The two methods will be tested in silico and their performances will be compared. Results from a simulation study indicate that it is possible to validate the case that one of the proposed models is more accurate for describing the temperature effect on the microbial growth rate. Both methods are able to design inputs with a sufficient discrimination potential. However, it has been observed that the Schwaab-approach provides inputs with a higher discrimination potential in combination with more accurate parameter estimates.