Machinability of ultrasonic vibration-assisted micro-grinding in biological bone using nanolubricant

Bone grinding is an essential and vital procedure in most surgical operations.Currently,the insufficient cooling capacity of dry grinding,poor visibility of drip irrigation surgery area,and large grinding force leading to high grinding temperature are the technical bottlenecks of micro-grinding.A new micro-grinding process called ultrasonic vibration-assisted nanoparticle jet mist cooling(U-NJMC)is innovatively proposed to solve the technical problem.It combines the advantages of ultrasonic vibration(UV)and nanoparticle jet mist cooling(NJMC).Notwithstanding,the combined effect of multi parameter collaborative of U-NJMC on cooling has not been investigated.The grinding force,friction coefficient,specific grinding energy,and grinding temperature under dry,drip irrigation,UV,minimum quantity lubrication(MQL),NJMC,and U-NJMC micro-grinding were compared and analyzed.Results showed that the minimum normal grinding force and tangential grinding force of U-NJMC micro-grinding were 1.39 and 0.32 N,which were 75.1%and 82.9%less than those in dry grinding,respectively.The minimum friction coefficient and specific grinding energy were achieved using U-NJMC.Compared with dry,drip,UV,MQL,and NJMC grinding,the friction coefficient of U-NJMC was decreased by 31.3%,17.0%,19.0%,9.8%,and 12.5%,respectively,and the specific grinding energy was decreased by 83.0%,72.7%,77.8%,52.3%,and 64.7%,respectively.Compared with UV or NJMC alone,the grinding temperature of U-NJMC was decreased by 33.5%and 10.0%,respectively.These results showed that U-NJMC provides a novel approach for clinical surgical micro-grinding of biological bone.

Calcium phosphate cements for bone engineering and their biological properties

Calcium phosphate cements （CPCs） are frequently used to repair bone defects. Since their discovery in the 1980s, extensive research has been conducted to improve their properties, and emerging evidence supports their increased application in bone tissue engineering. Much effort has been made to enhance the biological performance of CPCs, including their biocompatibility, osteoconductivity, osteoinductivity, biodegradability, bioactivity, and interactions with cells. This review article focuses on the major recent developments in CPCs, including 3D printing, injectability, stem cell delivery, growth factor and drug delivery, and pre- vascularization of CPC scaffolds via co-culture and tri-culture techniques to enhance angiogenesis and osteogenesis.

The biological function of type I receptors of bone morphogenetic protein in bone

Bone morphogenetic proteins （BMPs） have multiple roles in skeletal development, homeostasis and regeneration. BMPs signal via type I and type II serine/threonine kinase receptors （BMPRI and BMPRII）. In recent decades, genetic studies in humans and mice have demonstrated that perturbations in BMP signaling via BMPRI resulted in various diseases in bone, cartilage, and muscles. In this review, we focus on all three types of BMPRI, which consist of activin-like kinase 2 （ALK2, also called type IA activin receptor）, activin- llke kinase 3 （ALK3, also called BMPRIA）, and activin-like kinase 6 （ALK6, also called BMPRIB）. The research areas covered include the current progress regarding the roles of these receptors during myogenesis, chondrogenesis, and osteogenesis. Understanding the physiological and pathological functions of these receptors at the cellular and molecular levels will advance drug development and tissue regeneration for treating musculoskeletal diseases and bone defects in the future.