研究目的
The control of stability (or degradability) of materials is a strong and very prospective tool with huge potential in future biomedical use. Therefore, a lot of effort has been devoted to the research of parameters and processes that rule the degradation of materials to control aging and lifetime of objects used for healing and recovery.
研究成果
By selecting proper combinations of composition, structure and wettability, it is thus possible to prepare C:H:O plasma polymer ?lms with controlled degradability both in air and in water for potential use in biomedical applications such as drug delivery or as surface ?nish for implants.
研究不足
The technical and application constraints of the experiments, as well as potential areas for optimization.
1：Experimental Design and Method Selection:
Includes the overall experimental design rationale, the theoretical models or algorithms employed, and detailed procedures of the experimental methods.
2：Sample Selection and Data Sources:
Specifies the samples or datasets used in the experiment, including selection criteria and data acquisition methods.
3：List of Experimental Equipment and Materials:
Enumerates the required instruments, devices, and materials, along with their specifications and intended uses.
4：Experimental Procedures and Operational Workflow:
Provides a step-by-step description of the experimental process, covering equipment setup, data collection techniques, and control of variables during the experiment.
5：Data Analysis Methods:
Explains the approach for analyzing experimental data, including statistical techniques and software tools utilized.
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