Abstract: A detectable dust-proof paper is provided. The detectable dust-proof paper includes a detected layer, a first plastic layers, and a first ink-receptive layer. The detected layer has two opposite surfaces. The detected layer includes at least one metal which is selected from the group consisting of: aluminum, copper, nickel, iron, and a mixture or an alloy thereof. The first plastic layer is disposed on one of the two surfaces of the detected layer. A material of the first plastic layer is selected from the group consisting of: a polyolefin, a polyester, a polyamide, and any combination thereof. The first ink-receptive layer is disposed on the first plastic layer. The first ink-receptive layer contains an inorganic ink-absorption material ranging between a value larger than 0 wt % and 75 wt %.

Abstract: The present disclosure provides compounds with a hydrophilic self-immolative linker, which is cleavable under appropriate conditions and incorporates a hydrophilic group to provide better solubility of the compound. The compounds of the present disclosure comprise a drug moiety, a targeting moiety capable of targeting a selected cell population, and a linker which contains an acyl unit, an optional spacer unit for providing distance between the drug moiety and the targeting moiety, a peptide linker which can be cleavable under appropriate conditions, a hydrophilic self-immolative linker, and an optional second self-immolative spacer or cyclization self-elimination linker.

Abstract: A polyester film and a method for manufacturing the polyester film are provided. The method for manufacturing a polyester film by using a recycled plastic material includes the following steps. A part of the recycled plastic material is physically reproduced to obtain a physically regenerated polyester resin. Another part of the recycled plastic material is chemically reproduced to obtain a chemically regenerated polyester resin. A polyester composition including the physically regenerated polyester resin and the chemically regenerated polyester resin is prepared. Based on a total weight of the polyester composition being 100 wt %, a weight of the chemically regenerated polyester resin is larger than or equal to 5 wt %. The polyester film is manufactured by using the polyester composition. Based on a total weight of the polyester film being 100 wt %, a total amount of the physically regenerated polyester resin and the chemically regenerated polyester resin is from 10 wt % to 100 wt %.

Abstract: A car and a neighboring vehicle lane departure warning system and method are provided. The system includes a cloud server and a plurality of cars connected to the cloud server. Each car includes a vehicle body and a neighboring vehicle lane departure warning apparatus disposed on the vehicle body. The cloud server outputs a reminder signal to the cars within a specific distance of the neighboring vehicle after receiving a neighboring vehicle lane departure message, so that the drivers can be informed in time that the neighboring vehicle moves out of its lane, and can keep a proper distance from the neighboring vehicle in advance to prevent accidents.

Abstract: A PET synthetic paper is composed of a PET substrate and a soft ink absorbing coating coated on the PET substrate. The soft ink absorbing coating includes an acrylic coating and a polyurethane coating embossed on the acrylic coating. The acrylic coating has excellent printability and the polyurethane coating has velvety-soft tactility.

Abstract: A stretchable modified polyester film, and more particularly to a modified polyester film for in-mold decoration film and having high extensibility, high light transmittance, low shrinkage (high temperature resistance) and the like is provided. The stretchable polyester film is suitable to serve as a stretchable modified polyester film for an in-mold decoration film. The stretchable modified polyester film includes following components: (a) a polyester resin and (b) an acrylic resin.

Abstract: A PET synthetic paper is composed of a PET substrate and a soft ink absorbing coating coated on the PET substrate. The soft ink absorbing coating includes an acrylic coating and a polyurethane coating embossed on the acrylic coating. The acrylic coating has excellent printability and the polyurethane coating has velvety-soft tactility.

Abstract: A touch display apparatus and an operating method of the touch display apparatus are provided. An application icon is converted into a corresponding startup gesture icon if a touch operation conforms to an icon conversion operation. Here, the startup gesture icon indicates a gesture operation required for starting up an application corresponding to the startup gesture icon.

Abstract: The present disclosure provides compounds with a hydrophilic self-immolative linker, which is cleavable under appropriate conditions and incorporates a hydrophilic group to provide better solubility of the compound. The compounds of the present disclosure comprise a drug moiety, a targeting moiety capable of targeting a selected cell population, and a linker which contains an acyl unit, an optional spacer unit for providing distance between the drug moiety and the targeting moiety, a peptide linker which can be cleavable under appropriate conditions, a hydrophilic self-immolative linker, and an optional second self-immolative spacer or cyclization self-elimination linker.

Abstract: The present disclosure provides anti-folate receptor alpha (FRA) antibody-drug conjugates comprising a hydrophilic self-immolative linker. The present disclosures further provide compositions and methods for treating cancers.

Abstract: The present disclosure provides compounds with a hydrophilic self-immolative linker, which is cleavable under appropriate conditions and incorporates a hydrophilic group to provide better solubility of the compound. The compounds of the present disclosure comprise a drug moiety, a targeting moiety capable of targeting a selected cell population, and a linker which contains an acyl unit, an optional spacer unit for providing distance between the drug moiety and the targeting moiety, a peptide linker which can be cleavable under appropriate conditions, a hydrophilic self-immolative linker, and an optional second self-immolative spacer or cyclization self-elimination linker.

Abstract: The present disclosure provides compounds with a hydrophilic self-immolative linker, which is cleavable under appropriate conditions and incorporates a hydrophilic group to provide better solubility of the compound. The compounds of the present disclosure comprise a drug moiety, a targeting moiety capable of targeting a selected cell population, and a linker which contains an acyl unit, an optional spacer unit for providing distance between the drug moiety and the targeting moiety, a peptide linker which can be cleavable under appropriate conditions, a hydrophilic self-immolative linker, and an optional second self-immolative spacer or cyclization self-elimination linker.

Abstract: The present disclosure provides compounds with a hydrophilic self-immolative linker, which is cleavable under appropriate conditions and incorporates a hydrophilic group to provide better solubility of the compound. The compounds of the present disclosure comprise a drug moiety, a targeting moiety capable of targeting a selected cell population, and a linker which contains an acyl unit, an optional spacer unit for providing distance between the drug moiety and the targeting moiety, a peptide linker which can be cleaved under appropriate conditions, a hydrophilic self-immolative linker, and an optional second self-immolative spacer or cyclization self-elimination linker. In some aspects of the present disclosure, the targeting moiety is an anti-HER2 antibody. The present disclosure further provides compositions and methods for treating cancers.

Abstract: The present disclosure provides compounds with a hydrophilic self-immolative linker, which is cleavable under appropriate conditions and incorporates a hydrophilic group to provide better solubility of the compound. The compounds of the present disclosure comprise a drug moiety, a targeting moiety capable of targeting a selected cell population, and a linker which contains an acyl unit, an optional spacer unit for providing distance between the drug moiety and the targeting moiety, a peptide linker which can be cleavable under appropriate conditions, a hydrophilic self-immolative linker, and an optional second self-immolative spacer or cyclization self-elimination linker.

Abstract: The present disclosure provides anti-CD22 antibody-drug conjugates comprising a hydrophilic self-immolative linker. The present disclosures further provide compositions and methods for treating cancers.

Abstract: The present disclosure provides anti-folate receptor alpha (FRA) antibody-drug conjugates comprising a hydrophilic self-immolative linker. The present disclosures further provide compositions and methods for treating cancers.

Abstract: The present disclosure provides compounds with a hydrophilic self-immolative linker, which is cleavable under appropriate conditions and incorporates a hydrophilic group to provide better solubility of the compound. The compounds of the present disclosure comprise a drug moiety, a targeting moiety capable of targeting a selected cell population, and a linker which contains an acyl unit, an optional spacer unit for providing distance between the drug moiety and the targeting moiety, a peptide linker which can be cleavable under appropriate conditions, a hydrophilic self-immolative linker, and an optional second self-immolative spacer or cyclization self-elimination linker.

Abstract: A touch display apparatus and an operating method of the touch display apparatus are provided. An application icon is converted into a corresponding startup gesture icon if a touch operation conforms to an icon conversion operation.

Abstract: The present disclosure provides compounds with a hydrophilic self-immolative linker, which is cleavable under appropriate conditions and incorporates a hydrophilic group to provide better solubility of the compound. The compounds of the present disclosure comprise a drug moiety, a targeting moiety capable of targeting a selected cell population, and a linker which contains an acyl unit, an optional spacer unit for providing distance between the drug moiety and the targeting moiety, a peptide linker which can be cleavable under appropriate conditions, a hydrophilic self-immolative linker, and an optional second self-immolative spacer or cyclization self-elimination linker.

Abstract: The present disclosure provides compounds with a hydrophilic self-immolative linker, which is cleavable under appropriate conditions and incorporates a hydrophilic group to provide better solubility of the compound. The compounds of the present disclosure comprise a drug moiety, a targeting moiety capable of targeting a selected cell population, and a linker which contains an acyl unit, an optional spacer unit for providing distance between the drug moiety and the targeting moiety, a peptide linker which can be cleavable under appropriate conditions, a hydrophilic self-immolative linker, and an optional second self-immolative spacer or cyclization self-elimination linker.