Trends Anal. Chem. 165, 117156 (2023). Review of the use of radiolabeled pesticides to track nanoformulations in biological and environmental scenarios and the application of TLC for evaluating the mobility and degradation of pesticides and nanopesticides. The paper described TLC as tool to quantify the metabolites generated in the biodegradation study.

J. Planar Chromatogr. 35, 643-646 (2022). HPTLC of amitraz in visceral tissue on silica gel with hexane - acetone 4:1. Detection by spraying with 10 % sodium hydroxide solution, followed by heating at 80 °C for 10 min. The plate was then removed and kept for attaining room temperature, followed by spraying with freshly prepared sodium nitrite (1%) in acidic media. Right after, alkaline solution of curcumin (1% in sodium hydroxide solution) was sprayed. The hRF value for amitraz was 63. 

J. Liq. Chromatogr. Relat. Technol. 41, 1052-1065 (2019). Review of the following topics for the period of November 1, 2016 to November 1, 2018: sample preparation for TLC pesticide analysis; lipophilicity and retention studies for the study of biological activity; new reagents for pesticide detection; HPTLC-effect directed analysis on the surface of the layer; TLC-Raman spectrometry for the analysis of thiabendazole, triazophos, and phosmet residues; TLC analysis of radiolabeled pesticides; methods for the separation, detection, and qualitative and quantitative determination of pesticide residues; determination of pesticides in commercial products and the use of TLC for pesticide degradation studies. The review highlighted the isolation, characterization, and determination of less hazardous and less toxic biopesticides from plants, bacteria, fungi, and soil as the most active application area of pesticide TLC today.

J. Planar Chromatogr. 32(1), 51-53 (2019). TLC of amitraz in visceral tissues (stomach, intestine, liver, spleen, and kidney) on silica gel with hexane - acetone 4:1. Detection by spraying with 10 % sodium hydroxide solution, followed by heating at 80 °C for 10 min. The plate was then removed, kept to attain room temperature and sprayed with 5 % chloranil solution. The hRF values were between 49 and 51. The zones were stable for 8 h.

Lipids 17, 650-655 (1982). For preparative separation silica plates were used with hexane - ether 6:4. For separation of hydrogenated oils into their various components, multiple development (4 or 5x) TLC was carried out with ether - benzene 1:99 followed by ether - benzene 3:97. Analytical TLC components were visualized by charring with sulfuric acid-dichromate or with iodine vapors. reparative TLC: bands were located by spraying with ethanolic dichlorofluorescein, followed by viewing under UV. The components of the seed oil of trewia nudiflora and mallotus phillipinensis were chromatographed and compared.

J. A. O. A. C. 72, 512-514 (1989). TLC of 4 synthetic pyrethroids with a-cyano ester groups on silica with 6 different solvent systems. Detection by spraying with sodium hydroxide solution, p-nitrobenzaldehyde, o-dinitrobenzene solution, successively. Detection limits 0.1 µg.

J. Planar Chromatogr. 8, 160-161 (1995). TLC of the pyrethroid insecticides fenvalerate, cypermethrin, and deltamethrin on silica with petrol ether - ether 9:1. Detection after drying by successively spraying with 1% cobalt acetate and 5% sodium hydroxide, followed by spraying with 0.1% o-tolidine reagent after 5 min. Detection limit 10 µg.

CBS 90, 12-13 (2003). TLC of oxazoline Ia on aluminum sheets RP-18 with methanol over 10 mm, followed by water - acetonitrile 1:1 over 55 mm. Ion pair chromatography of oxazoline Ia with phosphate buffer - acetonitrile 1:1 over 60 mm after dipping in 2 mM cetyltrimethylammonium bromide. TLC of oxazoline Ib and Ic with phosphate buffer - acetonitrile - dioxane 4:3:3 over 65 mm. Determination by absorbance measurement at 200 nm (oxazoline Ia and Ib) and 262 nm (oxazoline Ic) respectively.