TY - JOUR
T1 - Technique for cellular microsurgery using the 193‐nm excimer laser
AU - Palanker, Daniel
AU - Ohad, Shoshanit
AU - Lewis, Aaron
AU - Simon, Alex
AU - Shenkar, Joseph
AU - Penchas, Shmuel
AU - Laufer, Neri
PY - 1991
Y1 - 1991
N2 - A new cell surgery technique has been developed to produce well‐defined alterations in cells and tissue without detectable heating and/or other structural damage in the surroundings. The technique involves the use of an argon fluoride excimer laser, in the deep ultraviolet (UV) region of the spectrum at 193 nm, which is guided through a glass pipette filled with a positive air pressure. To demonstrate the method, holes were drilled in the zona pellucida of mouse oocytes. The diameter of the drilled hole was determined by the pipette tip size, and its depth by an energy emitted per pulse and number of pulses. Scanning electron microscopy of the drilled mouse oocytes showed uniform, round, well‐circumscribed holes with sharp edges. Oocytes that had their zona pellucida drilled with this new method fertilized in vitro and developed to the blastocyst stage in a rate similar to that of control group. These results demonstrate the nonperturbing nature of this cold laser microsurgical procedure. In addition to the extension of our results for clinical in vitro fertilization purposes, such as enhancement of fertilization and embryo biopsy, there are wide‐ranging possible uses of our method in fundamental and applied investigations that require submicron accuracy in cellular alteration.
AB - A new cell surgery technique has been developed to produce well‐defined alterations in cells and tissue without detectable heating and/or other structural damage in the surroundings. The technique involves the use of an argon fluoride excimer laser, in the deep ultraviolet (UV) region of the spectrum at 193 nm, which is guided through a glass pipette filled with a positive air pressure. To demonstrate the method, holes were drilled in the zona pellucida of mouse oocytes. The diameter of the drilled hole was determined by the pipette tip size, and its depth by an energy emitted per pulse and number of pulses. Scanning electron microscopy of the drilled mouse oocytes showed uniform, round, well‐circumscribed holes with sharp edges. Oocytes that had their zona pellucida drilled with this new method fertilized in vitro and developed to the blastocyst stage in a rate similar to that of control group. These results demonstrate the nonperturbing nature of this cold laser microsurgical procedure. In addition to the extension of our results for clinical in vitro fertilization purposes, such as enhancement of fertilization and embryo biopsy, there are wide‐ranging possible uses of our method in fundamental and applied investigations that require submicron accuracy in cellular alteration.
KW - laser surgery
KW - microsurgery
KW - photoablation
KW - zona drilling
UR - http://www.scopus.com/inward/record.url?scp=0025833935&partnerID=8YFLogxK
U2 - 10.1002/lsm.1900110613
DO - 10.1002/lsm.1900110613
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C2 - 1753851
AN - SCOPUS:0025833935
SN - 0196-8092
VL - 11
SP - 580
EP - 586
JO - Lasers in Surgery and Medicine
JF - Lasers in Surgery and Medicine
IS - 6
ER -