Publications by authors named "Cai-fen Wang"

Article Synopsis
  • Cutaneous infections from non-tuberculous mycobacteria (NTM) are rare, particularly on the face, making diagnosis difficult due to their unique characteristics and the need for accurate microbial identification.
  • A case of a two-year-old boy with a growing reddish-brown facial mass revealed Mycobacterium avium complex infection, illustrating the importance of using imaging and microbiological methods for accurate diagnosis and treatment planning.
  • Ultrasound plays a key role in assessing the extent of cutaneous lesions and guiding interventions, but accurate diagnosis ultimately relies on confirming the specific pathogen involved.
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In conventional message communication systems, the practice of multi-message multi-receiver signcryption communication encounters several challenges, including the vulnerability to Key Generation Center (KGC) attacks, privacy breaches and excessive communication data volume. The KGC necessitates a secure channel to transmit partial private keys, thereby rendering the security of these partial private keys reliant on the integrity of the interaction channel. This dependence introduces concerns regarding the confidentiality of the private keys.

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The association rate constant and dissociation rate constant are important parameters of the drug-cyclodextrin supermolecule systems, which determine the dissociation of drugs from the complex and the further in vivo absorption of drugs. However, the current studies of drug-cyclodextrin interactions mostly focus on the thermodynamic parameter of equilibrium constants (K). In this paper, a method based on quantitative high performance affinity chromatography coupled with mass spectrometry was developed to determine the apparent dissociation rate constant (k(off,app)) of drug-cyclodextrin supermolecule systems.

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The release behavior of single pellet was investigated by LC/MS/MS method with tamsulosin hydrochloride (TSH) as the model drug of the research and then the pellets were divided into four groups according to the drug loading. Comparison of dissolution profiles of each group and capsule were performed using f1 and f2 factor methods to study the difference and similarity. The release profiles of single pellet, each group and capsule were analyzed using principle component analysis (PCA).

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