Cspc Zhongqi Pharmaceutical Technology (shijiazhuang) Co., Ltd.

Changzhou Bemate Home Technology Co., Ltd.

Nanjing University

Cspc Zhongqi Pharmaceutical Technology Co., Ltd.

Yanhui Li

Chunlei Li

Caixia Wang

Lan Zhang

Xiaoling Zhang

Zhiyuan Xiao

Dongmin Shen

Li Zhang

Min Liang

Yongfeng Li

Xian Xiu

Liang Peng

Lin Chen

Wenmin Guo

Yajuan Wang

Shixia Wang

Zhi Wang

Min Kang

Jinxu Wang

Dongjian Chen

Junxiang Dong

Hongmei Lin

Shasha Yang

Shujie Yan

Xuefang Xia

Meng Zhou

Likun Liu

A deep learning-based Java program internal annotation generation method and system is provided. The method includes acquiring items with a Stars number ranked in the top, and extracting corresponding internal annotations and method statement lists; obtaining an <annotation, target code> pair; selecting an annotation in a Verb-dobj form; obtaining a code context associated with a target code segment; preprocessing the annotation, the target code, and the context to obtain a triplet dataset; randomly dividing the constructed dataset into a training set, a validation set, and a test set, and constructing an encoder-decoder network at the same time; enabling the training set in division to be used for model training, performing evaluation on the validation set to obtain a model with the best effect on the validation set as a target model; and predicting data in the test set with the obtained target model to generate a predicted annotation.

Deep learning-based java program internal annotation generation method and system

The disclosure relates to the manufacturing of floors, and more particularly to a polypropylene board and a method for preparing the same. The polypropylene board is prepared from 25-40 parts by weight of a modified polypropylene resin, 30-70 parts by weight of a filler, 3-10 parts by weight of a stabilizer and 1-8 parts by weight of a lubricant. A melt flow rate of the modified polypropylene resin is 2-9 g/10 min.

Polypropylene board and method for preparing same

Disclosed herein are an antimicrobial reinforced floor and a method for preparing the same. In the method, a substrate and an impregnated paper impregnated with an inorganic antimicrobial agent and an organic antimicrobial agent are subjected to hot press forming to produce the antimicrobial reinforced floor.

Antimicrobial reinforced floor and method for preparing same

A floor coating, which is prepared from 55-70% by weight of an epoxy-modified polyurethane resin, 5-10% by weight of AlO, 10-25% by weight of SiC, 0.4-1% by weight of a leveling agent, 0.3-1% by weight of a dispersant, 5-10% by weight of a solvent and 0.2-0.8% by weight of a curing agent. A degree of polymerization of the epoxy-modified polyurethane resin is 80-100. A scratch-resistant floor and a preparation method thereof are also disclosed herein.

Scratch-resistant floor and method for producing same, and floor coating

A liposome comprising bilayer and inner water phase is disclosed. Said inner water phase may contain sulfobutyl ether cyclodextrin and an active compound.

Liposome having inner water phase containing sulfobutyl ether cyclodextrin salt

Purified therapeutic nanoparticles are provided herein. Such nanoparticles comprise an active pharmaceutical ingredient and human serum albumin, wherein the weight ratio of human serum albumin to the active ingredient in the therapeutic nanoparticles is from 0.01:1 to 1:1, and wherein the nanoparticles are substantially free of free human serum albumin that is not incorporated in the nanoparticles. The present disclosure also provides pharmaceutical compositions that comprise the purified therapeutic nanoparticles and are also substantially free of free human serum albumin. Methods for preparing and using the purified therapeutic nanoparticles and compositions thereof are also provided.

Purified therapeutic nanoparticles and preparation methods thereof

The present invention relates to a liposomal pharmaceutical preparation containing a multivalent ionic drug, a process for the preparation of the liposomal pharmaceutical preparation, and a use thereof in the treatment of diseases, in which the liposome has a size of about 30-80 nm, and the phospholipid bilayer has a phospholipid with a Tm higher than body temperature, so that the phase transition temperature of the liposome is higher than the body temperature.

Liposomal pharmaceutical preparation and method for manufacturing the same

A liposome comprising bilayer and inner water phase is disclosed. Said inner water phase contains sulfobutyl ether cyclodextrin and active compound. Said sulfobutyl ether cyclodextrin is sulfobutyl ether &#x3b1;-cyclodextrin, sulfobutyl ether &#x3b2;-cyclodextrin, or sulfobutyl ether &#x3b3;-cyclodextrin.

Growing community of inventors

Jiangsu, China

Yanhui Li