Most compounding and concentrates executives contacted by Plastics News expect the solid growth rates of 2018 to continue into 2019.

Survivors include two daughters and sons-in-law, April and Chip Gwyn of Powder Springs, and Summer and Paul Parks of Indianapolis, Ind.; two sons and one daughter-in-law, Jeffery and Crystal Kimbrell of Hiram, and Timothy Kimbrell of Rockmart; two sisters and one brother-in-law, Katheryn and Gary Lemley of Rockmart, and Lillian Robertson of Cedartown; one brother and sister-in-law, Lee and Melissa Davis of Temple; nine grandchildren, Alexa Kimbrell, Reese Kimbrell, Presleigh Kimbrell, Alexis Kimbrell, Autumn Bagley, Ethan Gwyn, Peyton Parks, Cannon Parks and Bryson Parks; and a number of other relatives.

“After the five-year not-giving-up effort and with a great teamwork using a combination of X-ray powder diffraction analysis and crystal structure prediction algorithms, we solved the crystal structure of the new polymorph,” Dr. Hu said.

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Survivors include her Daughter and son in law, Pamela and Terry Hindman; daughter in law, Edith Brownlow Mills; grandchildren: Jeremy and Rebecca Hindman, Nicholas Hindman and Kaci Mills; great grandchildren: Abby Hindman, Megan Hindman, Kyler Hindman and Levi Hindman; sister, Edna Rexroth. Several nieces and nephews also survive.

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The Waitemata Harbour has long run grey with the ashes of boaties whose last wish was to be at one with the sea or swim with the fishes. It is a Hindu purifying ritual to release ashes into flowing water. But the custom offends Maori, for whom water is both a life-giving force and valued food source that must be sustained.

I ended up in the emergency room with the worst pain I’ve ever had in my life. They did all sorts of tests — EKGs, CT scans, ultrasound, bloodwork — thinking it might be a heart attack or gastrointestinal problem. Everything came back near perfect, except that they found portal hypertension of the liver.

The formal consultation attracted just 12 submissions and the Funeral Directors Association will be one of the few to represent the living at the hearing on Monday week. "We should have been consulted and now we’ve missed the submissions deadline," Shanti Patel says. "That’s the biggest issue."

The MGT substrate with high reproducibility, sensitivity, and selectivity was then developed as an immunoassay SERS probe (MGT-Abs-CuPc) through the immobilization of the PD-L1 Abs and CuPc for PD-L1 analysis on TNBC surfaces (Fig. 5A). As shown in fig. S5A, upon the introduction of CuPc molecules to MGT, the UV-vis spectrum exhibits two peaks at 620 and 690 nm, which correspond to the adsorption of CuPc. After the immobilization of Abs to MGT, we observed an additional peak at ~260 nm, which should be attributed to adsorption of Abs. All these three additional peaks show the successful fabrication of the MGT-Abs-CuPc nanoprobe. To further confirm Abs conjugation to the nanostructures, we performed SDS–polyacrylamide gel electrophoresis (PAGE) imaging of MGT, Abs, and Abs-modified MGT (MGT-Abs). SDS-PAGE is a powerful analytical technique for protein identification in complex biological samples and has been widely used in biological studies for decades. As shown in fig. S5B, MGT-Abs [fig. S5B (III)] was higher than both MGT [fig. S5B (I)] and Abs [fig. S5B (II)], indicating the different molecular weights: MGT-Abs > MGT > Abs. SDS-PAGE imaging in fig. S5B (I to III) definitively showed the successful conjugation between the nanostructure and Abs. In addition, we also carried out FTIR spectroscopy (fig. S5C) to investigate the conjugation. Compared to MGT, MGT-Abs showed an additional infrared band assigned to the C–N stretching vibration at 1400 cm−1 and the C=O stretching vibration at 1620 cm−1. These two additional peaks were attributed to the formation of an amide bond at the interface between MGT and Abs. Both SDS-PAGE images and FTIR results revealed that Abs has been successfully conjugated to the nanostructures. We carried out confocal imaging to verify the recognition ability of MGT-Abs to the PD-L1 protein. We conducted three parallel experiments, which are shown in fig. S5 (D to G). No fluorescence signal was obtained after the coincubation of MGT and Cy5-labeled PD-L1. Moreover, before incubating with Cy5-labeled PD-L1, MGT-Abs also showed weak fluorescence. However, after the incubation with Cy5-labeled PD-L1, confocal images exhibited a bright fluorescence signal, indicating the high affinity and recognition ability of MGT-Abs to the PD-L1 protein. We incubated the developed probe with high SERS activity with TNBCs to quantify the PD-L1 expression on the surface of different TNBCs (Fig. 5A) using Raman spectroscopy. Temperature and incubation time are two important factors that determine the overall SERS signals. As shown in fig. S5 (H and I), the maximum SERS response was achieved at 37°C and 60 min. The amount of CuPc and Abs immobilized on MGT was another important experimental parameter. As the concentration of CuPc and Abs progressively increased, we observed the Raman peak at 1530 cm−1 to first increase and then decrease after the concentration reached 10 mM for CuPc and 100 μM for Abs, indicating that the optimal concentration of CuPc is 10 mM, while that of Abs is 100 μM (fig. S5, J and K). Moreover, we examined the cytotoxicity of the MGT-Abs-CuPc probe with a 3-(4,5-dimethylthiazol-2-yl)-2-diphenyltetrazolium bromide assay. As a result, the variability of HCC38, MDA-MB-231, and MCF-7 cells remained approximately 98% (15 μM, 120 min; fig. S6), indicating the low cytotoxicity of the probe. After optimizing experimental conditions and assessing biocompatibility, we conducted three parallel experiments to evaluate the PD-L1 expression levels on three different types of TNBC (HCC38, MCF-7, and MDA-MB-231) surfaces. HCC38 cells were first used as model cells. As shown in Fig. 5B, Raman intensity increased with an increasing number of cells captured on the silicon foil. The intensity of the Raman peak at 1530 cm−1 was used to reflect the amount of the MGT-Abs-CuPc probe attached to the cell surface. The intensity of the Raman peak (I) was proportional to the logarithmic value of captured cancer cells (N) in the range from 5 × 102 to 5 × 105 cells (R = 0.990, n = 7; Fig. 5C), which was consistent with the kinetics mechanism of the antigen-Abs reaction in the Abs excess zone (fig. S7A). The linear regression is shown in Eq. 1

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